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IL179167A - Compounds which act on 11bhsd1, pharmaceutical compositions comprising them and their use - Google Patents

Compounds which act on 11bhsd1, pharmaceutical compositions comprising them and their use

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Publication number
IL179167A
IL179167A IL179167A IL17916706A IL179167A IL 179167 A IL179167 A IL 179167A IL 179167 A IL179167 A IL 179167A IL 17916706 A IL17916706 A IL 17916706A IL 179167 A IL179167 A IL 179167A
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IL
Israel
Prior art keywords
thiazol
alkyl
amino
ylamino
bicyclo
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IL179167A
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IL179167A0 (en
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Biovitrum Ab
Amgen Inc
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Priority claimed from SE0401324A external-priority patent/SE0401324D0/en
Priority claimed from SE0402509A external-priority patent/SE0402509D0/en
Priority claimed from PCT/US2005/018081 external-priority patent/WO2005116002A2/en
Application filed by Biovitrum Ab, Amgen Inc filed Critical Biovitrum Ab
Publication of IL179167A0 publication Critical patent/IL179167A0/en
Publication of IL179167A publication Critical patent/IL179167A/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D277/28—Radicals substituted by nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/48—Nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/38—Nitrogen atoms
    • C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/10—Spiro-condensed systems
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    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Description

179167/2 179167 [7'Ji I 453580 mx wi» v>m OJM o>v n o am Novel compounds which acts on lipHSDl, pharmaceutical composition comprising them and their use Amgen Inc.
Biovitrum AB C. 171126 INHIBITORS OF 11-BETA-HYBROXY STEROID DEHYDROGENASE TYPE 1 CROSS-REFERENCE TO RELATED PATENT APPLICATIONS
[0001] This application claims priority to Swedish Patent Application No. 0401324-9, filed May 24, 2004, Swedish Patent Application No. 0402509-4, filed October 15, 2004, and U.S. Provisional Patent Application No. 60/650,777, filed January 31 , 2005.
FIELD OF THE INVENTION
[0002] The present invention relates to novel compounds, to pharmaceutical compositions comprising the compounds, as well as to the use of the compounds in medicine and for the preparation of a medicament which acts on the human 11 -β-hydroxysteroid dehydrogenase type 1 enzyme (11 PHSDl).
BACKGROUND OF THE INVENTION
[0003] Hydroxysteroid dehydrogenases (HSDs) regulate the occupancy and activation of steroid hormone receptors by converting steroid hormones into" their inactive metabolites. For a recent review, see Nobel et al., Eur. J. Biochem. 2001, 268:41 13-4125.
[0004] There exist numerous classes of HSDs. The 11-beta-hydroxysteroid dehydrogenases (11 β -HSDs) catalyze the interconversion of active glucocorticoids (such as Cortisol and corticosterone), and their inert/forms (such as cortisone and 11-dehydrocorticosterone). The isoform 11-beta-hydroxysteroid dehydrogenase type 1 (11/3-HSD1) is expressed in liver, adipose tissue, brain, lung and other glucocorticoid tissue and is a potential target for therapy directed at numerous disorders that may be ameliorated by reduction of glucocorticoid action, such as diabetes, obesity and age-related cognitive dysfunction. Seckl, et al., Endocrinology, 2001, 142:1371-1376.
[0005] The various isozymes of the 17-beta-hydroxysteroid dehydrogenases (1 Ίβ-HSDs) bind to androgen receptors or estrogen receptors and catalyze the interconversion of various sex hormones including estradiol/estrone and testosterone/androstenedione. To date, six isozymes have been identifed in humans and are expressed in various human tissues including endometrial tissue, breast tissue, colon tissue, and in the testes. 17-beta-Hydroxysteroid dehydrogenase type 2 (173-HSD2) is expressed in human endometrium and its activity has been reported to be linked to cervical cancer. itawaki et al., J. Clin.
Endocrin. Metab., 2000, 85: 1371-3292-3296. 17-beta-Hydroxysteroid dehydrogenase type 3 (17/S-HSD3) is expressed in the testes and its modulation may be useful for the treatment of androgen-related disorders.
[0006] Androgens and estrogens are active in their 17/3-hydroxy configurations, whereas their 17-keto derivatives do not bind to androgen and estrogen receptors and are thus inactive. The conversion between the active and inactive forms (estradiol/estrone and testosterone/androstenedione) of sex hormones is catalyzed by members of the 17/3-HSD family. 17/3-HSDl catalyzes the formation of estradiol in breast tissue, which is important for the growth of malignant breast tumors. Labrie et al., Mol. Cell. Endocrinol. 1991 , 78:C113-Cl 18. A similar role has been suggested for 17/3-HSD4 in colon cancer. English et al., J. Clin. Endocrinol. Metab. 1999, 84:2080-2085. 17/3-HSD3 is almost exclusively expressed in the testes and converts androstenedione into testosterone. Deficiency of this enzyme during fetal develoment leads to male pseudohermaphroditism. Geissler et al., Nat. Genet. 1994, 7:34-39. Both 17/3-HSD3 and various 3a-HSD isozymes are involved in complex metabolic pathways which lead to androgen shuffles between inactive and active forms. Penning et al., Biochem. J. 2000, 351:67-77. Thus, modulation of certain HSDs can have potentially beneficial effects in the treatment of androgen- and estrogen-related disorders.
[0007] The 20-alpha-hydroxysteroid dehydrogenases (20a-HSDs) catalyze the interconversion of progestins (such as between progesterone and 20a-hydroxy progesterone).
Other Substrates for 20oHSDs include 1 TrV-hvHrnv /nrecmprinln .** hydroxyprogesterone, leading to 20a-OH steroids. Several 20o>HSD isoforms have been identified and 20a-HSDs are expressed in various tissues, including the placenta, ovaries, testes and adrenals. Peltoketo, et al., J. Mol. Endocrinol. 1999, 23:1-11.
[0008] The 3-alpha-hydroxysteroid dehydrogenases (3oc-HSDs) catalyze the interconversion of the androgens dihydrotestosterone (DHT) and 5a-androstane-3o 17/3-diol and the interconversion of the androgens DHEA and androstenedione and therefore play an " important role in androgen metabolism. Ge et al., Biology of Reproduction 1999, 60:855-860. 1. Glucorticoids, diabetes and hepatic glucose production
[0009] It has been known for more than half a century that glucocorticoids have a central role in diabetes. For example, the removal of the pituitary gland or the adrenal gland from a diabetic animal alleviates the most severe symptoms of diabetes and lowers the concentration of glucose in the blood (Long, CD. and Leukins, F.D.W. (1936) J. Exp. Med. 63: 465-490; Houssay, B.A. (1942) Endocrinology 30: 884-892). It is also well established that glucocorticoids enable the effect of glucagon on the liver.
[0010] The role of 11 HS I as an important regulator of local glucocorticoid effect and thus of hepatic glucose production is well substantiated (see, e.g., Jamieson et al. (2000) J. Endocrinol. 165: 685-692). Hepatic insulin sensitivity was improved in healthy human volunteers treated with the non-specific 1 l HSDl inhibitor carbenoxolone (Walker, B. . et al. (1995) J. Clin. Endocrinol. Metab. 80: 3155-3159). Furthermore, the expected mechanism has been established by different experiments with mice and rats. These studies showed that the rnRNA levels and activities of two key enzymes in hepatic glucose production were reduced, namely: the rate-limiting enzyme in gluconeogenesis, phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6-phosphatase (G6Pase) the enzyme catalyzing the last common step of gluconeogenesis and glycogenolysis. Finally, blood glucose levels and hepatic glucose production are reduced in mice in which the 1 l HSDl gene is knocked-out. Data from this model also confirm that inhibition of 1 lpHSDl will not cause hypoglycemia, as predicted since the basal levels of PEPCK and G6Pase are regulated independently of glucocorticoids (Kotelevtsev, Y. et al., (1997) Proc. Natl. Acad. Sci. USA 94: 14924-14929).
[0011] FR 2,384,498 discloses compounds having a high hypoglycemic effect.
Therefore, treatment of hyperglycemia with these compounds may lead to hypoglycemia. 2. Possible reduction of obesity and obesity related cardiovascular risk factors
[0012] Obesity is an important factor in syndrome X as well as in the majority (> 80%) of type 2 diabetes, and omental fat appears to be of central importance. Abdominal obesity is closely associated with glucose intolerance, hyperinsulinemia, hypertriglyceridemia, and other factors of the so-called syndrome X (e.g. increased blood pressure, decreased levels of HDL and increased levels of VLDL) (Montague & O'Rahilly, Diabetes 49: 883-888, 2000). Inhibition of the l ip'HSDl enzyme in pre-adipocytes (stromal cells) has been shown to decrease the rate of differentiation into adipocytes. This is predicted to result in diminished expansion (possibly reduction) of the omental fat depot, i.e., reduced central obesity (Bujalska, I.J., S. Kumar, and P.M. Stewart (1997) Lancet 349: 12104213).
[0013] Inhibition of 11 HSDI in mature adipocytes is expected to attenuate secretion of the plasminogen activator inhibitor 1 (PAI-1) - an independent cardiovascular risk factor (Halleux, CM. et al. (1999) J. Clin. Endocrinol. Metab. 84: 4097-4105).
Furthermore, there is a clear correlation between glucocorticoid "activity" and cardiovascular risk factor suggesting that a reduction of the glucocorticoid effects would be beneficial (Walker, B.R. et al. (1998) Hypertension 31 : 891-895"; Fraser, R. et al. (1999) Hypertension 33: 1364-1368).
[0014] Adrenalectomy attenuates the effect of fasting to increase both food intake " and hypothalamic neuropeptide Y expression. This supports the role of glucocorticoids in promoting food intake and suggests that inhibition of 1 ipHSDl in the brain might increase satiety and therefore reduce food intake (Woods, S.C. et al. (1998) Science, 280: 1378-1383). 3. Possible beneficial effect on the pancreas
[0015] Inhibition of 1 l HSDl in isolated murine pancreatic β-cells improves ■ glucose-stimulated insulin secretion (Davani, B. et al. (2000) J. Biol. Chem. 2000 Nov 10; 275(45): 34841-4). Glucocorticoids were previously known to reduce pancreatic insulin release in vivo (Billaudel, B. and B.CJ. Sutter (1979) Horm. Metab. Res. 1 1 : 555-560). Thus, inhibition of 1 l HSDl is predicted to yield other beneficial effects for diabetes treatment, besides the effects on liver and fat.
[0016] Stress and glucocorticoids influence cognitive function (de Quervain, D.J.-F., B. Roozendaal, and J.L. McGaugh (1998) Nature 394: 787-790). The enzyme l i HSDl controls the level of glucocorticoid action in the brain and thus contributes to neurotoxicity (Rajan, V., C.R.W. Edwards, and J.R. Seckl, J. (1996) Neuroscience 16: 65-70; Seckl, J.R., Front. (2000) Neuroendocrinol. 18: 49-99). Unpublished results indicate significant memory improvement in rats treated with a non-specific 1 l HSDl inhibitor (J. Seckl, personal communication). Based the above and on the known effects of glucocorticoids in the brain, it may also be suggested that inhibiting 1 l HSDl in the brain may result in reduced anxiety (Tronche, F. et al. (1999) Nature Genetics 23: 99-103). Thus, taken together, the hypothesis is that inhibition of 1 lpHSDl in the human brain would prevent reactivation of cortisone into Cortisol and protect against deleterious glucoc'orticoid-mediated effects on neuronal survival and other aspects of neuronal function, including cognitive impairment, depression, and increased appetite.
. Possible use of immuno-modulation using l i HSDl inhibitors
[0017] The general perception is that glucocorticoids suppress the immune system. But in fact there is a dynamic interaction between the immune system and the HPA (hypothalamo-pituitary-adrenal) axis (Rook, G.A.W. (1999) Baillier's. Clin. Endocrinol. Metab. 13: 576-581). The balance between the cell-mediated response and humoral responses is modulated by glucocorticoids. A high glucocorticoid activity, such as at state of stress, is associated with a humoral response. Thus, inhibition of the enzyme 1 ipHSDl has been suggested as a means of shifting the response towards a cell-based reaction. , [0018] In certain disease states, including tuberculosis, lepra and psoriasis the immune reaction is nomialy biased towards a humoral response when in fact the appropriate response would be cell based. Temporal inhibition of 1 ipHSDl, local or systemic, might be used to push the immune system into the appropriate response (Mason, D. (1991) Immui ology Today- 12: 57-60; Rook et al., supra).
[0019] An analogous use of 1 ipHSDl inhibition, in this case temporal, would be to booster the immune response in association with immunization to ensure that a cell based response would be obtained, when desired. 6. Reduction of intraocular pressure : [0020] Recent data suggest that the levels of the glucocorticoid target receptors and the 1 l HSD enzymes determines the susceptibility to glaucoma (Stokes, J. et al. (2000) Invest. Ophthalmol. 41 : 1629-1638). Further, inhibition of l i pHSDl was recently presented as a novel approach to lower the intraocular pressure (Walker E. A. et al, poster P3-698 at the Endocrine society meeting June 12-15, 1999, San Diego). Ingestion of carbenoxolone, a non-specific inhibitor, of l ipHSDl, was shown to reduce the intraocular pressure by 20% in normal subjects; In the eye; expression of l ipHSDl is confined to basal cells of the corneal epithelium and the non-pigmented epithelialium of the cornea (the site of aqueous production), to ciliary muscle and to the 'sphincter and dilator muscles of the iris. In contrast, the distant isoenzyme 1 ipHSD2 is highly expressed in the non-pigmehted ciliary epithelium and corneal endothelium. None of the enzymes is found at the trabecular meshwork, thfe site of drainage. Thus, 1 lj3HSDl is suggested to have a role in aqueous production, rather than drainage, but it is presently unknown if this is by interfering with activation of the glucocorticoid or the mineralocorticoid receptor, or both. 7. Reduced osteoporosis
[0021] Glucocorticoids have an essential role in skeletal development and function ' but are detrimental in excess. Glucocorticoid-induced bone loss is derived, at least in part, via inhibition of bone formation, which includes suppression of osteoblast proliferation and collagen synthesis (Kim, C.H., Cheng, S.L. and Kim, G.S. (1999) J. Endocrinol. 162: 371-379). The negative effect on bone nodule formation could be blocked by the non-specific inhibitor carbenoxolone suggesting an important role of li HSDl in the glucocorticoid effect (Bellows, C.G., Ciaccia, A. and Heersche, J.N.M. (1998) Bone 23: 119-125). Other data suggest a role of 11 ^HSDl in providing sufficiently high levels of active glucocorticoid in osteoclasts, and thus in augmenting bone resorption (Cooper, M.S. et al. (2000) Bone 27: 375-381). Taken together, these different data suggest that inhibition of 1 I HSDl may have beneficial effects against osteoporosis by more than one mechanism working in parallel. 8. Reduction of hypertension
[0022] Bile acids inhibit 1 lB-hydroxysteroid dehydrogenase type 2. This results in a shift in the overall body balance in favour of Cortisol over cortisone, as shown by studying tne ratio oi me urinary mexaooines ^uauru am, v ugi, o., uuram u, ., Ιη λ, ., .^, B.M., Frey, FJ. (2001) J Clin Invest. Nov;108(9): 1299-305. "Reduced activity of llbeta-hydroxysteroid dehydrogenase in patients with cholestasis".). Reducing the activity of 1 lbHSDl in the liver by a selective inhibitor is predicted to reverse this imbalance, and acutely counter the symptoms such as hypertension, while awaiting surgical treatment removing the biliary obstruction.
[0023] WO 99/65884 discloses carbon substituted aminothiazole inhibitors of cyclin dependent kinases. These compounds may, e.g., be used against cancer, inflammation and arthritis. US 5,856,347 discloses an antibacterial preparation or bactericide comprising 2-aminothiazole derivative and/or salt thereof. Further, US 5,403,857 discloses benzenesulfonamide derivatives having 5 -lipoxygenase inhibitory activity. Additionally, tetrahydrothiazolo[5,4-c]pyridines are disclosed in: Analgesic tetrahydrothiazolo[5,4- c]pyridines. Fr. Addn. (1969), 18 pp, Addn. to Fr. 1498465. CODEN: FAXXA3; FR 94123 19690704 CAN 72: 100685 AN 1970:100685 CAPLUS and 4,5,6,7-Tetrahydrothiazolo[5,4-cjpyridines. Neth. Appl. (1967), 39 pp. CODEN: NAXXAN NL 6610324 19670124 CAN 68:49593, AN 1968: 49593 CAPLUS. However, noiie of the above disclosures discloses the compounds according to the present invention, or their use for the treatment of diabetes, obesity, glaucoma, osteoporosis, cognitive disorders, irnmune disorders, depression, and hypertension.
[0024] WO 98/16520 discloses compounds inhibiting matrix metalloproteinases (MMPs) and TNF-a converting enzyme (TACE). EP 0 749 964 Al and US 5,962,490 disclose compounds having an endothelin receptor antagonist activity. WO 00/02851 discloses compounds associated with a disturbed cGMP balance. None of these compounds fall within formula (I) according to the present invention. Furthermore, nothing is said about the activity on l i pHSDl. [00251 US 5,783,697 discloses thiophene derivatives as inhibitors of PGE2 and LTB4. Nothing is said about the activity on l ipHSDl.
[0026] EP 0 558 258, EP 0 569 193, and EP 1 069 114 disclose isoxazole derivatives as endothelin agonists and antagonists. Nothing is said about the activity on l ipHSDl. 9. Wound healing
[0027] Cortisol performs a broad range of metabolic functions and other functions. The multitude of glucocorticoid action is exemplified in patients with prolonged increase in plasma glucocorticoids, so called "Cushing's syndrome". Patients with Cushing's syndrome have prolonged increase in plasma glucocorticoids and exhibit impaired glucose tolerance, type 2 diabetes, central obesity, and osteoporosis. These patients also have impaired wound healing and brittle skin (Ganong, W.F. Review of Medical Physiology. Eighteenth edition ed. Stamford, Connecticut: Appleton & Lange; 1997).
[0028] Glucocorticoids have been shown to increase risk of infection and delay healing of open wounds (Anstead, G.M. Steroids, retinoids, and wound healing. Adv Wound Care 1998;1 l(6):277-85). Patients treated with glucocorticoids have 2-5-fold increased risk of complications when undergoing surgery (Diethelm, A.G. Surgical management of complications of steroid therapy. Ann Surg 1977; 185(3):251 -63).
[0029] The European patent application No. EP 0902288 discloses a method for diagnosing the status of wound healing in a patient, comprising detecting Cortisol levels in said wound. The authors suggest that elevated levels of Cortisol in wound fluid, relative to normal plasma levels in healthy individuals, correlates with large, non-healing wounds (Hutchinson, T.C., Swaniker, H.P., Wound diagnosis by quantitating Cortisol in wound fluids. European patent application No. EP 0 902 288, published 17.03.1999).
[0030] Bi humans, the 11 β-HSD catalyzes the conversion of Cortisol to cortisone, and vice versa. The parallel function of 11 β-HSD in rodents is the interconversion of corticosterone and 11-dehydrocorticosterone (Frey, F.J., Escher, G., Frey, B.M.
Pharmacology of 11 beta-hydroxysteroid dehydrogenase. Steroids 1994;59(2):74-9). Two isoenzymes of 1 Ιβ-HSD, 1 Ιβ-HSDl and 1 i -HSD2, have been characterized, and differ from each other in function and tissue distribution (Albiston, A.L., Obeyesekere, V.R., Smith, R.E., Krozowski, Z.S. Cloning and tissue distribution of the human 11 beta-hydroxysteroid dehydrogenase type 2 enzyme. Mol Cell Endocrinol 1994;105(2):R11-7). Like GR, 11β-HSD1 is expressed in numerous tissues like liver, adipose tissue, adrenal cortex, gonads, lung, pituitary, brain, eye etc (Monder C, White PC. 11 beta-hydroxysteroid dehydrogenase. Vitam Horm 1993;47: 187-271; Stewart, P.M., Krozowski, Z.S. 11 beta-Hydroxysteroid dehydrogenase. Vitam Horm 1999;57:249-324; Stokes, J., Noble, J., Brett, L., Phillips, C, Seckl, J.R., O'Brien, C, et al. Distribution of glucocorticoid and mineralocorticoid receptors Ophthalmol Vis Sci 2000;41(7):1629-38). The function of 1 Ιβ-HSDl is to fine-tune local glucocorticoid action. 1 Ιβ-HSD activity has been shown in the skin of humans and rodents, in human fibroblasts and in rat skin pouch tissue (Hammami, M.M., Siiteri, P.K. Regulation of 11 beta-hydroxysteroid dehydrogenase activity in human skin fibroblasts: enzymatic modulation of glucocorticoid action. J Clin Endocrinol Metab 1991;73(2):326-34); Cooper, M.S., Moore, J., Filer, A., Buckley, CD., Hewison, M., Stewart, P.M. 11 beta-hydroxysteroid dehydrogenase in human fibroblasts: expression and regulation depends on tissue of origin. ENDO 2003 Abstracts 2003; Teelucksingh, S., Mackie, A.D., Burt, D., Mclntyre, M.A., Brett, L., Edwards, C.R. Potentiation of hydrocortisone activity in skin by glycyrrhetinic acid. Lancet 1990;335(8697):1060-3; Slight, S.H., Chilakamarri, V.K., Nasr, S., Dhalla, A. ., S Ramires, F.J., Sun, Y., et al. Inhibition of tissue repair by spironolactone: role of mineralocorticoids in fibrous tissue formation. Mol Cell Biochem 1998; 189(1 -2):47-54).
[0031] Wound healing consists of serial events including inflammation, fibroblast proliferation, secretion of ground substances, collagen production, angiogenesis, wound contraction and epithelialization. It can be divided in three phases; inflammatory, proliferative and remodeling phase (reviewed in Anstead et al., supra).
[0032] In surgical patients, treatment with glucocorticoids increases risk of wound infection and delay healing of open wounds. It has been shown in animal models that restraint stress slows down cutaneous wound healing and increases susceptibility to bacterial infection during wound healing. These effects were reversed by treatment with the glucocorticoid receptor antagonist RU486 (Mercado, A.M., Quan, N., Padgett, D.A., Sheridan, J.F., Marucha, P.T. Restraint stress alters the expression of interleukin-1 and keratinocyte growth factor at the wound site: an in situ hybridization study. J Neuroimmunol 2002; 129(1 -2): 74-83; Rojas, I.G., Padgett, D.A., Sheridan, J.F., Marucha, P.T. Stress-induced susceptibility to bacterial infection during cutaneous wound healing. Brain Behav Immun 2002;16(l):74-84). Glucocorticoids produce these effects by suppressing inflammation, decrease wound strength, inhibit wound contracture and delay epithelialization (Anstead et al., supra). Glucocorticoids influence wound healing by interfering with production or action of cytokines and growth factors like IGF, TGF-β, EGF, KGF and PDGF (Beer, H.D., Fassler, R., Wemer, S.
Glucocorticoid-regulated gene expression during cutaneous wound repair. Vitam Horm 2000;59:217-39; Hamon, G.A., Hunt, T.K., Spencer, E.M. In vivo effects of systemic insulinlike growth factor-I alone and complexed with insulin- like growth factor binding protein-3 on corticosteroid suppressed wounds. Growth Regul 1993;3(l):53-6; Laato, M., Heino, J., Kahari, V.M., Niinikoski, J., Gerdin, B. Epidermal growth factor (EGF) prevents methylprednisolone-induced inhibition of wound healing. J Surg Res 1989;47(4):354-9; Pierce, G.F., Mustoe, T.A., Lingelbach, J., Masakowski, V.R., Gramates, P., Deuel, T.F. Transforming growth factor beta reverses the glucocorticoid-induced wound-healing deficit in rats: possible regulation in macrophages by platelet-derived growth factor. Proc Natl Acad Sci U S A 1989;86(7):2229-33). It has also been shown that glucocorticoids decrease collagen synthesis in rat and mouse skin in vivo and in rat and human fibroblasts (Oishi, Y., Fu, Z.W., Ohnuki, Y., Kato, H., Noguchi, T. Molecular basis of the alteration in skin collagen metabolism in response to in vivo dexamethasone treatment: effects on the synthesis of 179167/2 collagen type I and III, collagenase, and tissue inhibitors of metalloproteinases. Br J Dermatol 2002; 147(5):859-68).
[0033] WO 01/90090 discloses thiazole compounds, which compounds inhibit the human 1 Ιβ-HSDl, and may be useful for treating disorders such as diabetes, obesity, glaucoma, osteoporosis, cognitive disorders and immune disorders. Other 1 Ιβ-HSDl inhibitors are disclosed in e.g. WO 01/90091 ; WO 01/90092; WO 01/90093; WO 01/90094; WO 03/043999; WO 03/044000; WO 03/044009; U.S. Patent Publication No. 2005/009821; WO 04/103980; WO 04/1 12784; WO 04/112781 ; WO 04/112785; WO 04/112783; WO 04/112782; WO 04/113310; WO 04/112779; and Swedish patent application No. SE 0400227-5, filed on February 4, 2004. However, the use of the 1 1β- HSD1 inhibitors according to the present invention for diabetes, obesity, glaucoma, osteoporosis, cognitive disorders, immune disorders, and wound healing has not previously been disclosed.
[0034] Although not disclosed as 1 Ιβ-HSDl inhibitors, Okawara et al. disclose the preparation of thiazole-5-spiropropan-4(5H)-ones, see J. Chem. Soc. Perkin Trans. I, 1733- 1735 (1986).
SUMMARY OF THE INVENTION An an aspect, the invention provides a compound of the general formula (III): wherein: Pv5 is optionally substituted phenyl-(CR10aR10a)1-3-; and wherein R10a is methyl, fluoro or RIO and R10a may combine together to form a C3-C6- cycloalkyl ring; 179167/2 R6 is C1-8-alkyl, C]-8-alkoxy, C3.i0-cycloalkyl, heterocyclyl, CMo-cycloalkyl-Ci. 8-alkyl, CN-Ci-8-alkyl, aryl, aryl-Ci-s-alkyl, heterocyclyl-C1-8-alkyl or haloalkyl; R7 is -NR8R9, halo, Ci-8-alkyl, -(CR8R9)n-OR8, -S-Ci-C8-alkyl, C3-10-cycloalkyl, heterocyclyl, C3-i0-cycloalkyl-C]-8-alkyl, cyano-C1-8-alkyl, aryl, aryl-Ci-8-alkyl, heterocyclyl-C i -8-alkyl, heterocyclyl-C(0)-C i -8-alkyl, heterocyclyl-S02-C i -8- alkyl, Ci-g-haloalkyl, HO-Ci-g-alkyl, -C(O)-C3-Ci0-cycloalkyl, -C(0)-C1-C8-haloalkyl, -(CR8R9)n-Y-(CR8R9)n-heterocyclyl or -(CR8R9)n-Y- (CR8R9)n-C(0)-R8, wherein n is 0-5, Y is NR10, 0 or S; wherein any aryl, alkyl, heterocyclyl or cycloalkyl residue is optionally substituted by one or more of -d-Cg-alkyl, -halo, -OH, -OR10, C1-C8-alkyl-S02-, -S02-aryl, -C(0)-(CR8R9)n-carbamate, -C(0)-0-C!-C8-alkyl, -C(0)-Ci-C8-alkyl, -C(0)-(CR8R9)n-C(0)-NR8R9, -C(0)-(CR8R9)n-NR8-C(0)-Ci-C8-alkyl -C(0)-(CR8R9)n-NR8R9, -C(0)-C3-Cio-cycloalkyl, 179167/2 -C(0)-aryl, -C(0)-(CR8R9)n-heterocyclyl, -C C8 alkyl-OR8, -C(0)-halo-C1-C8-alkyl or wherein any aryl, alkyl, cycloalkyl, or heterocyclyl residue is optionally independently substituted by one or more C1-8-alkyl, aryl, halogen, -NR10R10, d-Cg-haloalkyl, HO-d-Cg-alkyl, d-Cg-alkyl-OR10, -OR10, (C3-C10)-cycloalkyl, d-Cg-alkyl-sulfonyl, -0-(CR8R9)n-heterocyclyl, -O-(CR8R9)n-C(0)-NR8R9, -0-(CR8R9)n-NR8R9, -Y-(CR8R9)n-NR8-C(0)-d-C8-alkyl, -Y-(CR8R )n-heterocyclyl, or d-C8-alkyl-S02; wherein R and R are each independently hydrogen, d-C8 alkyl, d-Cg alkoxy, -NR10R10, -S-(d-C8)alkyl, aryl or heterocyclyl; any alkyl, alkoxy, heterocyclyl or aryl may be substituted with one to three substituents being -halo, unsubstituted d-Cg alkyl, unsubstituted d-Cg alkoxy, unsubstituted d-Cgthioalkoxy or unsubstituted aryl(d-C4)alkyl; wherein R10 is independently hydrogen, d-Cg alkyl, aryl-d-Cg alkyl, d-Cg alkoxy, -S-(Ci-C8)alkyl, heterocyclyl or aryl; any alkyl, heterocyclyl or aryl may be substituted with one to three substituents being -halo, unsubstituted d-Cg alkyl, unsubstituted d-Cg alkoxy, unsubstituted d-Cg thioalkoxy or unsubstituted aryl(d-C4)alkyl; or R6 and R7 form, together with the carbon atom bonded thereto, a saturated, partially unsaturated or unsaturated C3-1o-cycloalkyl or a saturated, partially unsaturated or unsaturated C4-d4 heterocyclyl; 179167/2 wherein the cycloalkyl or the heterocyclyl may be optionally substituted by one or more of Ci-C8-alkyl, aryl, Cj-Cg-haloalkyl, aryl-Ci-C8-alkyl, C3-C10- cycloalkyl, -OR8, -0, =NR8, =N-OR8, -NR8R9, -SR8, -halo, -OC(0)R8, - C(0)R8, -C02R8, -CONR8R9, -OC(0)NR8R9, -NR9C(0)R8, -NR8C(0)NR8R9, - NR8S02NR8R9, -NR8C02R9, -NHC(NH2)=NH, -NR8C(NH2)=NH, - NHC(NH2)=NR8, -S(0)R8, -S02R8, -S02NR8R9, -NR8S02R9, -CN or -N02; and pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers and N-oxides thereof, with the proviso that: when R and R combine to form a cyclopropyl ring, then R is not benzyl.
In some embodiments, R5 is (optionally substituted phenyl)-(C(CH3)2)-, (optionally substituted phenyl)-(CHCH3), or benzyl.
In another aspect, the invention provides a compound of the general formula wherein: R5 is Ci-Cg alkyl, C3-10-cycloalkyl, C3-10-cycloalkyl-Ci-8-alkyl, aryl, aryl-Ci-g- alkyl, heterocyclyl, or haloalkyl; wherein any aryl, cycloalkyl, or heterocyclyl residue is optionally independently substituted by one or more C1-8-alkyl, aryl, halogen, halo-C]-C8-alkyl, HO-CrCg- alkyl, d-Cg-alkyl-OR10, -OR10, (C3-C10)-cycloalkyl or Cj-Cg- alkyl-sulfonyl; 179167/2 R6 is Ci-C8 alkyl, C3-C10 cycloalkyl, saturated or partially unsaturated heterocyclyl, heteroaryl or aryl; R7 is -NR8R9, halo, Ci-8-alkyl, -S-C C8-alkyl, C3-i0-cycloalkyl, heterocyclyl, C3- io-cycloalkyl-C1-8-alkyl, cyano-C1-8-alkyl, aryl, aryl-Ci-8-alkyl, heterocyclyl-Ci-8- alkyl, heterocyclyl-C(0)-C1-8-alkyl, heterocyclyl-S02-C1-8-alkyl, alkyl, -C(O)-C3-C10-cycloalkyl, -C(0)-Cr-C8-haloalkyl, -(CR8R9)n-Y-(CR8R9)n- heterocyclyl or -(CR8R9)n-Y-(CR8R9)n-C(0)-R8 (wherein n is 0-5, Y is NR10, 0 or S); wherein any aryl, alkyl, heterocyclyl or cycloalkyl residue is optionally substituted one or more of -Ci-C8-alkyl, -halo, CrCs-alkyl-SOr, -S02-aryl, -C(0)-(CR8R9)n-carbamate, -C(0)-0-C C8-alkyl, -C(0)-Ci-C8-alkyl, -C(0)-(CR8R9)n-C(0)-NR8R9, -C(0)-(CR8R9)n-NR8-C(0)-C1-C8-alkyl -C(0)-(CR8R9)n-NR8R9, -C(O)-C3-C10-cycloalkyl, -C(0)-aryl, -C(0)-(CR8R9)n-heterocyclyl, 179167/2 -CrC8 alkyl-OR8, -C(0)-halo-CrCg-alkyl or -C(0)-(CR8R9)n-aryl, wherein any aryl, alkyl, cycloalkyl, or heterocyclyl residue is optionally independently substituted by one or more C1-8-alkyl, aryl, halogen, -NR10R10, d- C8-haloalkyl, HO-Ci-Cg-alkyl, d-Cg-alkyl-OR10, -OR10, (C3-C10)-cycloalkyl, d-Cg-alkyl-sulfonyl, -0-(CR8R9)n-heterocyclyl, -0-(CR8R9)n-C(0)-NR8R9, -0-(CR8R9)n-NR8R9, -Y-(CR8R9)n-NR8-C(0)-d-C8-alkyl, -Y-(CR8R9)n-heterocyclyl, or d-Cg-alkyl-S02; wherein R and R are each independently hydrogen, d-Cg alkyl, d-Cg alkoxy, - NR10R10, -S-(d-C8)alkyl, aryl or heterocyclyl; any alkyl, alkoxy, heterocyclyl or aryl may be substituted with one to three substituents being from -halo, unsubstituted Cj-Cg alkyl, unsubstituted d-Cg alkoxy, unsubstituted d-C thioalkoxy and unsubstituted aryl(d-C4)alkyl; wherein R10 is independently hydrogen, d-Cg alkyl, aryl-d-Cg alkyl, d-Cg alkoxy, -S-(C1-C8)alkyl, heterocyclyl or aryl; any alkyl, heterocyclyl or aryl may be substituted with one to three substituents being -halo, unsubstituted d-Cg alkyl, unsubstituted d-C8 alkoxy, unsubstituted d-C8 thioalkoxy or unsubstituted aryl(C1-C4)alkyl; or R6 and R7 form, together with the carbon atom bonded thereto, a saturated, partially unsaturated or unsaturated C3-10-cycloalkyl or a saturated, partially unsaturated or unsaturated C4-C14 heterocyclyl; wherein the cycloalkyl or the heterocyclyl may be optionally substituted by one or more of d-Cg-alkyl, aryl, d-Cg-haloalkyl, aryl-d-Cg-alkyl, C3-Ci0-cycloalkyl, -OR8, =0, =NR8, =N-OR8, -NR8R9, -SR8, -halo, -OC(0)R8, -C(0)R8, -C02R8, - C0NR8R9, -0C(0)NR8R9, -NR9C(0)R8, -NR8C(0)NR8R9, -NR8S02NR8R9, - NR8C02R9, -NHC(NH2)=NH, -NR8C(NH2)=NH, -NHC(NH2)=NR8, -S(0)R8, - S02R8, -S02NR8R9, -NR8S02R9, -CN and -N02; and pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers and N-oxides thereof, with the proviso that: when R =R =methyl, then R is not phenyl or 4-iodophenyl, R =R =phenyl, then R is not phenyl, and R and R combine to form a cyclopropyl ring, then R is not n-butyl, cyclohexyl, benzyl, phenyl or naphthyl; or a compound which is 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2. l]hept-2-ylamino)-5-ethyl-l ,3-thiazol-4(5H)-one; 2-(bicyclo[2 ^]hept-2-ylamino)-5-phenyl-l,3-thiazol-4(5H)-one; 2-(cyclohexylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 2-(bicyclo[2 ]hept-2-ylamino)-5,5-dimethyl-l,3-thiazol-4(5H)-one; - Isopropyl-2-(tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l,3-thiazol-4(5H)-one; 6- (tricyclo [3.3.1.0-3 ,7~]non-3-ylamino)-5 -thia-7-azaspiro [3.4] oct-6-en-8-one; 2-(Tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l,3-thiazol-4(5H)-one; 6-(Cyclooctylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-(Cycloheptylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-(Bicyclo[2.2.1]hept-2-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 179167/2 6-[(2,2,3,3-Tetramethylcyclopropyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-[(2-Methylphenyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-[(cyclohexylmethyl)amino]-5,5-dimethyl-l,3-thiazol-4(5H)-one; 2-[(2-fluorophenyl)amino]-5-isopropyl-l,3-thiazol-4(5H)-one; 2- [(cyclohexylmethyl)amino] -5-(2-hydroxyphenyl)- 1 ,3 -thiazol-4(5H)-one; (5S)-2-(cycloheptylamino)-5-methyl-l,3-thiazol-4(5H)-one; (5R)-2-(cycloheptylamino)-5-methyl-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; -tert-butyl-2-(cyclohep1ylainino)-l33-thiazol-4(5H)-one; 2-(cyclooc1ylamino)-5-ethyl-l,3-thiazol-4(5H)-one; -isopropyl-2-[(2-isopropylphenyl)amino]-l,3-thiazol-4(5H)-one; -ethyl-2- [(2-isopropylphenyl)amino] - 1 ,3-thiazol-4(5H)-one; 2-[(2-chlorophenyl)amino]-5-ethyl-l,3-thiazol-4(5H)-one; -ethyl-2-[(2-methylphenyl)amino]-l,3-thiazol-4(5H)-one; -isopropyl-2-[(2,2,3,3-te1xamethylcyclopropyl)amino]-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1 ]hept-2-ylamino)-5-(4-hydroxybenzyl)- 1 ,3-thiazol-4(5H)-one; -[(cyclohexylmethyl)amino]-4-thia-6-azaspiro[2.4]hept-5-en-7-one; -(cycloheptylamino)-5-(3,4-dihydroxybenzyl)-l,3-thiazol-4(5H)-one; -(cycloheptylamino)-5-( 1 H-imidazol-4-ylmethyl)- 1 ,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-isobutyl- 1 ,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-(lH-indol-3-ylmethyl)-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-(4-hydroxybenzyl)-l,3-thiazol-4(5H)-one; (5 ?)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-l,3-tluazol-4(5H)-one; 2-(cyclooctylamino)-5-(4-hydroxybenzyl)- 1 ,3-thiazol-4(5H)-one; (5S)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-l,3-thiazol-4(5H)-one; [2-(cycloheptylamino)-4-oxo-4,5-dihydro-l,3-tWazol-5-yl]acetonitrile; 2-(cycloheptylamino)-5-(pyridin-3-ylmethyl)- 1 ,3-thiazol-4(5H)-one; - Isopropyl-2-[(2-methylphenyl)amino]-l,3-thiazol-4(5H)-one; 2-(Cyclooctylamino)-5,5-dimethyl- 1 ,3-thiazol-4(5H)-one; 2-(Cyclooctylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; 2-(Bicyclo[2.2.1]hept-2-ylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2-(Tricyclo[3 ~3,7~]non-3-ylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4 2-(Cycloheptylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2-(Cyclooctylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2- { [1 -(4-Chlorophenyl)cyclobutyl]amino} -5-isopropyl- 1 ,3 -thiazol-4(5H)-o 6- {[l-(4-Chlorophenyl)cyclobutyl]amino}-5-thia-7-azaspiro[3.4]oct-6-en-i 2-(cycloheptylamino)-5,5-diethyl-l,3-thiazol-4(5H)-one; (5S)-5-isopropyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5R)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; 179167/2 (5S)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5R)-5-isopropyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5 S)-5-isopropyl-2- { [(2R)-2-phenylpropyl] amino } - 1 ,3 -thiazol-4(5H)-one; (5R)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5S)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; 2-Anilino-5-isopropyl-l,3-thiazol-4(5H)-one; -Isopropyl-2-[(2-morpholin-4-ylethyl)ammo]-l,3-thiazol-4(5H)-one; 2-(Bicyclo[2.2.1]hept-2-ylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 2-(Cycloheptylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 2-(Cyclooctylamino)- 1 -thia-3-azaspiro[4.4]non-2-en-4-one; 2-[(2,2,3,3-Tetramethylcyclopropyl)ammo]-l-thia-3-azaspiro[4.4]non-2-en-4-one; or pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides thereof.
In another embodiment, R6 is Q-Cg alkyl.
In a further embodiment, R6 is methyl, ethyl, n-propyl or iso-propyl.
In yet another embodiment, the invention provides a compound according to another aspect which is: 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1]hept-2-ylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1]hept-2-ylamino)-5-phenyl-l,3-thiazol-4(5H)-one; 2-(cyclohexylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1]hept-2-ylamino)-5,5-dimethyl-l,3-thiazol-4(5H)-one; .0~3,7~]non-3-ylamino)-l,3-thiazol-4(5H)-one; 6- (tricyclo[3.3.1.0~3,7~]non-3-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-(Tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l ,3-thiazol-4(5H)-one; 6-(Cyclooctylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-(Cycloheptylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-(Bicyclo[2.2.1]hept-2-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-[(2,2,3,3-Tetramethylcyclopropyl)amino]-5-lJiia-7-azaspiro[3.4]oct-6-en-8-one; 6-[(2-Methylphenyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-[(cyclohexylmethyl)amino]-5,5-dimethyl-l,3-thiazol-4(5H)-one; 2-[(2-fluorophenyl)amino]-5-isopropyl-l,3-thiazol-4(5H)-one; 2- [(cyclohexylmethyl)amino] -5-(2-hydroxyphenyl)- 1 ,3 -thiazol-4(5H)-one; (5S)-2-(cycloheptylamino)-5-methyl- 1 ,3-thiazol-4(5H)-one; (5R)-2-(cycloheptylamino)-5-methyl- 1 ,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; -te^butyl-2-(cycloheptylamino)-l,3-thiazol-4(5H)-one; 2-(cyclooctylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 179167/2 -isopropyl-2-[(2-isopropylphenyl)amino]-l,3-thiazol-4(5H)-one; -ethyl-2- [(2-isopropylphenyl)amino] - 1 ,3 -thiazol-4(5H)-one; 2-[(2-chlorophenyl)amino]-5-ethyl-l,3-thiazol-4(5H)-one; -ethyl-2- [(2-methylphenyl)amino] - 1 ,3 -thiazol-4(5H)-one; -isopropyl-2- [(2,2,3 ,3 -tetramethylcyclopropyl)amino]- 1 ,3 -thiazol-4(5H)-one; 2-(bicyclo[2.2.1 ]hept-2-ylamino)-5-(4-hydroxybenzyl)- 1 ,3-thiazol-4(5H)-one; -[(cyclohexylmethyl)amino]-4-thia-6-azaspiro[2.4]hept-5-en-7-one; 2-(cycloheptylamino)-5-(3,4-dihydroxybenzyl)-l,3-tniazol-4(5H)-one; 2-(cycloheptylamino)-5-(lH-imidazol-4-ylmethyl)-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-isobutyl-l,3-tbiazol-4(5H)-one; 2-(cycloheptylamino)-5-( 1 H-indol-3-ylmethyl)- 1 ,3-thiazol-4(5H)-one; 2-(cyclohep1ylamino)-5-(4-hydroxybenzyl)-l,3-thiazol-4(5H)-one; (5i?)-2-(cycloheptylamino)-5-(cyclohexylmethyl)- 1 ,3-thiazol-4(5H)-one; 2-(cyclooctylamino)-5-(4-hydroxybenzyl)-l,3-thiazol-4(5H)-one; (5S)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-l,3-thiazol-4(5H)-one; [2-(cycloheptylamino)-4-oxo-4,5-dihydro-l,3-tbiazol-5-yl]acetonitrile; 2-(cyclohep1ylamino)-5-(pyridin-3-ylmethyl)-l,3-thiazol-4(5H)-one; -Isopropyl-2-[(2-methylphenyl)amino]-l,3-thiazol-4(5H)-one; 2-(Cyclooctylamino)-5,5-dimethyl-l,3-thiazol-4(5H)-one; 2-(Cyclooctylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; 179167/2 2-(Bicyclo [2.2.1 ]hept-2-ylamino)- 1 -thia-3 -azaspiro [4.5]dec-2-en-4-one; 2-(Tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2-(Cycloheptylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2-(Cyclooctylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2-{[l-(4-CUorophenyl)cyclobu1yl]amino}-5-isopropyl-l,3-thiazol-4(5H)-one; 6- { [ 1 -(4-Chlorophenyl)cyclobutyl]amino} -5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-(cycloheptylamino)-5,5-diethyl-l,3-thiazol-4(5H)-one; (5 S)-5-isopropyl-2- { [(2S)-2-phenylpropyl] amino } - 1 ,3 -thiazol-4(5H)-one; (5R)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5 S)-5-ethyl-2- { [(2S)-2-phenylpropyl]amino} - 1 ,3 -thiazol-4(5H)-one; (5R)-5-isopropyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5 S)-5 -isopropy 1-2- { [(2R)-2-phenylpropyl] amino } - 1 ,3 -thiazol-4(5 H)-one ; (5R)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5S)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; 2-Anilino-5-isopropyl- 1 ,3-thiazol-4(5H)-one; -Isopropyl-2-[(2-morpholin-4-ylethyl)amino]-l,3-thiazol-4(5H)-one; 2-(Bicyclo[2.2.1]hept-2-ylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 2-(Cycloheptylamino)- 1 -thia-3-azaspiro[4.4]non-2-en-4-one; 2-(Cyclooctylamino)- 1 -thia-3-azaspiro[4.4]non-2-en-4-one; 179167/2 2- [(2,2,3 ,3 -Tetramethylcyclopropyl)amino] - 1 -thia-3 -azaspiro [4.4]non-2-en-4- one; or pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides thereof.
In a further aspect the invention provides a pharmaceutical formulation comprising a compound as defined according to the invention, in combination with a pharmaceutically acceptable diluents or carrier.
In some embodiments, the formulation is formulated for oral delivery.
In other embodiments, the oral delivery is in the form of a tablet.
In still a further aspect, the invention provides use of the compound as defined in the invention for the manufacture of a medicament for the prophylaxis or treatment of a 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder or for achieving immune-modulation.
In some embodiments, the disorder is diabetes, syndrome X, obesity, glaucoma, hyperlipidemia, hyperglycemia, hyperinsulinemia, hypertension, osteoporosis, dementia, depression, virus diseases, or inflammatory diseases.
In some embodiments, the use according to the invention for the treatment of prophylaxis of a medical condition involving delayed or impaired wound healing.
In other embodiments, the medical condition involving delayed or impaired wound healing is diabetes.
In further embodiments, the medical condition involving delayed or impaired wound healing is caused by treatment with glucocorticoids.
In still further embodiments, the promotion of wound healing in chronic wounds, said wounds being diabetic ulcers, venous ulcers or pressure ulcers. 179167/2 In some additional embodiments, the immune-modulation is tuberculosis, lepra, or psoriasis.
In a further aspect, the invention provides use of the compound of the invention for the manufacture of a medicament for inhibiting 11-β-hydroxysteroid dehydrogenase type 1 enzyme in a subject.
In some embodiments the compound according to another aspect which is: 2-[l-(4-Fluoro-phenyl)-emylamino]-5-memyl-5-(tetrahydro-pyran-4-ylmethyl)- thiazol-4-one; (5S)-5-((l-acetyl-4-piperidinyl)methyl)-2-((lS,4R)-bicyclo[2.2.1]hept-2-ylamino)- 5-methyl-l ,3-thiazol-4(5H)-one; (5R)-2-((l S,4R)-bicyclo[2.2.1]hept-2-ylamino)-5-methyl-5-(tetrahydro-2H-pyran-4- ylmethyl)-l,3-thiazol-4(5H)-one; (5S)-2-((l S,4R)-bicyclo[2.2.1 ]hept-2-ylamino)-5-methyl-5-tetrahydro-2H-pyran-4- yl l,3-thiazol-4(5H)-one; 2-((lR,2R,4S)-bicyclo[2.2.1]hept-2-ylamino)-8-oxa-l-thia-3-azaspiro[4.5]dec-2-en- 4-one; (5S)-2-((lS,4R)-bicyclo[2.2.1]hept-2-ylamino)-5-((l-(3-furanylcarbonyl)-4- piperidinyl)methyl)-5-methyl-l,3-thiazol-4(5H)-one; 2-(l-Cyclohexyl-ethylamino)-5-isopropyl-5-methyl-thiazol-4-one; 2-(5,5-Difluoro-bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-5-methyl-lJ iazol-4-one; 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-5-methyl-thiazol-4-one; 2-[l-(2-Trifluoromethyl-phenyl)-ethylamino]-8-oxa-l-thia-3-aza-spiro[4.5]dec-2- en-4-one; 179167/2 (5R)-2-((l S,2S,4R)-bicyclo[2.2.1 ]hept-2-ylamino)-5-methyl-5-(trifluoromethyl)- l,3-thiazol-4(5H)-one; 2-(Bicyclo[2 ]hept-2-ylamino)-5-(l-fluoro-l-methyl-ethyl)-5-methyl-thiazol-4- one; 2-[l-(4-Fluoro-phenyl)-ethylamino]-5-methyl-5-pyridin-4-yl-thiazol-4-one; -Methyl-5-pyridin-4-yl-2-[l-(2-1xifluoromethyl-phenyl)-ethylamino]-thiazol-4-one; 2-[l-(2-Fluoro-phenyl)-ethylamino]-5-methyl-5-pyridin-4-yl-thiazol-4-one; -(1 -Fluoro- 1 -methyl-ethyl)-2- [ 1 -(2-fluoro-phenyl)-ethylamino] -5-methyl-thiazol- 4-one; 2-[l-(2-Fluoro-phenyl)-ethylamino]-5-met yl-5-trifluoromethyl-thiazol-4-one; -( 1 , 1 -Difluoro-ethyl)-2- [ 1 -(4-fluoro-phenyl)-ethylamino] -5-methyl-thiazol-4-one; 2- [ 1 -(2-Chloro-phenyl)-ethylamino] -5-methyl-5-trifluoromethyl-thiazol-4-one; 2-[l-(4-Fluoro-phenyl)-ethylarnino]-5-methyl-5-trifluoromethyl-thiazol-4-one; 2-[l-(4-Fluoro-phenyl)-ethylamino]-5-(2-methoxy-pyridin-4-yl)-5-me1liyl-thiazol-4- one; -( 1 -Fluoro- 1 -methyl-ethyl)-2-[ 1 -(4-fluoro-phenyl)-ethylamino]-5-methyl-thiazol- 4-one, (S)-2-((lR,2R,4R)-5-hydroxybicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one, (S)-2-((lR,2S,4R)-5-hydroxybicyclo[2.2.1]heptan-2-ylamino)-5- isopropyl-5- methylthiazol-4(5H)-one, (S)-2-((l S,2S,4R)-6-hydroxybicyclo[2.2. l]heptan-2-ylamino)-5- isopropyl-5- methylthiazol-4(5H)-one, 179167/2 (S)-2-((l S,2S,4R)-bicyclo[2.2. l]heptan-2-ylamino)-5-((R)-l- hydroxypropan-2-yl)- 5-methylthiazol-4(5H)-one, (S)-2-((l S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-((S)-l- hydroxypropan-2-yl)- 5-methylthiazol-4(5H)-one, (S)-2-((l S,2S,4R)-bicyclo[2.2. l]heptan-2-ylamino)-5-(2-hydroxypropan-2-yl)-5- methylthiazol-4(5H)-one, (S)-2-((l S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piOp-l-en-2- yl)thiazol-4(5H)-one, (S)-2-((lR,2S,4R)-5-hydroxybicyclo[2.2.1]heptan-2-ylamino)-5- isopropyl-5- methylthiazol-4(5H)-one, or pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tauiomers, optical isomers or N-oxides thereof.
In another aspect, the invention provides a process for the preparation of a compound as defined in the invention comprising the following reacting scheme: wherein: X is S; and LG is a leaving group.
In a further aspect, the invention provides a process for the preparation of pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides of a compound as defined in claim 1 or 3, comprising the following reaction scheme: wherein: X is S; and LG is a leaving group; thereby yielding said compound and converting same to said pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides, thereof.
In another embodiment, the LG is halide, tosylate, mesylate or triflate.
In some embodiments, the chiral base is a chiral lithium base.
In another aspect, the invention provides a compound that is 2- (Cyclooctylamino)-5,5-dimemyl-l,3-thiazol-4(5H)-one or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof.
In one embodiment the compound is 5-ethyl-2-[(2-isopropylphenyl)amino]-l,3-thiazol-4(5H)-one or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof. 179167/2 In a further embodiment, the compound is 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-5-methyl-thiazol-4-one or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof.
In an additional embodiment, the copoud is (S)-2-((lR,2R,4R)-5-hydroxybicyclo[2.2. l]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof.
All passages of the description which are outside the scope of the claims do not constitute part of the claimed invention. 179167/2 DETAILED DESCRIPTION OF THE INVENTION
[0317] The compounds according to the present invention may be used in several indications which involve 11 -β-hydroxysteroid dehydrogenase type 1 enzyme. Thus, the compounds according to the present invention may be used against dementia (see WO97/07789), osteoporosis (see Canalis, E. 1996, Mechanisms of glucocorticoid action in bone: implications to glucocorticoid-induced osteoporosis, Journal of Clinical Endocrinology and Metabolism, 81, 3441-3447) and may also be used for disorders in the immune system (see Franchimont et al, "Inhibition of Thl immune response by glucocorticoids: dexamethasone selectively inhibits IL-12-induced Stat 4 phosphorylation in T lymphocytes", The journal of Immunology 2000, Feb 15, vol 164 (4), pages 1768-74) and also in the above listed indications.
[0318] The various terms used, separately and in combinations, in the above definition of the compounds having the Formula (I), (II), (III) and (IV) will be explained.
[0319] The term "aryl" in the present description is intended to include aromatic rings (monocyclic or bicyclic) having from 6 to 10 ring carbon atoms, such as phenyl (Ph), naphthyl, and indanyl (i. e., 2,3-dihydroindenyl), which optionally may be substituted by Ci- 6-alkyl. Examples of substituted aryl groups are benzyl, and 2-methylphenyl.
[0320] The term "heteroaryl" means in the present description a monocyclic, bi- or tricyclic aromatic ring system (only one ring need to be aromatic) having from 5 to 14, preferably 5 to 10 ring atoms such as 5, 6, 7, 8, 9 or 10 ring atoms (mono- or bicyclic), in which one or more of the ring atoms are other than carbon, such as nitrogen, sulfur, oxygen and selenium as part of the ring system. Examples of such heteroaryl rings are pyrrole, imidazole, thiophene, furan, thiazole, isothiazole, thiadiazole, oxazole, isoxazole, oxadiazole, pyridine, pyrazine, pyrimidine, pyridazine, pyrazole, triazole, tetrazole, chroman, isochroman, quinoline, quinoxaline, isoquinoline, phthalazine, cinnoline, quinazoline, indole, isoindole, benzothiophene, benzofuran, isobenzofuran, benzoxazole, 2,1,3-benzoxadiazole, benzopyrazole; benzothiazole, 2, 1,3 -benzothiazole, 2,1,3-benzoselenadiazole, benzimidazole, indazole, benzodioxane, indane, 1,5-naphthyridine, 1,8-naphthyridine, acridine, fenazine and xanthene.
[0321] The term "heterocyclic" and "heterocyclyl" in the present description is intended to include unsaturated as well as partially and fully saturated mono-, bi- and tricyclic rings having from 4 to 14, preferably 4 to 10 ring atoms having one or more heteroatoms (e.g., oxygen, sulfur, or nitrogen) as part of the ring system and the reminder being carbon, such as, for example, the heteroaryl groups mentioned above as well as the corresponding partially saturated or fully saturated heterocyclic rings. Exemplary saturated heterocyclic rings are azetidine, pyrrolidine, piperidine, piperazine, morpholine, tetrahydroquinoline, 1,2,3,4-tetrahydroisoquinoline, 3,4-dihydro-2H-l ,4-benzoxazine, hexahydroazepine, 3,4-dihydro-2(lH)isoquinoline, 2,3-dihydro-lH-indole, l,3-dihydro-2H-isoindole, azocane, l-oxa-4-azaspiro[4.5]dec-4-ene, decahydroisoquinoline, and 1,4-diazepane. In addition, the heterocyclyl or heterocyclic moiety may optionally be substituted with one or more oxo groups.
[0322] Ci.g-alkyl in the compound of formula (I) according to the present application may be a straight or branched alkyl group containing 1-8 carbon atoms.
Exemplary alkyl groups include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, isopentyl, hexyl, isohexyl, n-heptyl, and n-octyl. For parts of the range "C -alkyl" all subgroups thereof are contemplated such as Ci-7-alkyl, C1-6-alkyl, C^s-alkyl, C1. -alkyl, C2-8-alkyl, C2-7-alkyl, C2-6-alkyl, C2.5-alkyl, C3-7-alkyl, C4-6-alkyl, etc. 34
[0323] Ci .g-alkoxy in the compound of formula (I) according to the present application may be a straight or branched alkoxy group containing 1 -8 carbon atoms.
Exemplary alkoxy groups include methoxy, ethoxy, propoxy, isopropoxy, butoxy, sec-butoxy, tert-butoxy, pentyloxy, isopentyloxy, hexyloxy, isohexyloxy, n-heptyloxy, and n-octyloxy. For parts of the range "C].6-alkoxy" all subgroups thereof are contemplated such as Ci-7-alkoxy, Ci-6-alkoxy, Ci-5-alkoxy, Ci-4-aIkoxy, C2.s-alkoxy, C2-7-alkoxy, C2-6-alkoxy, C2. 5-alkoxy, C3-7-alkoxy, C4-6-alkoxy, etc.
[0324] C]_8-acyl in the compound of formula (I) according to the present application may be a straight or branched acyl group containing 1-8 carbon atoms. Exemplary acyl groups include formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, n-hexanoyl, n-heptanoyl, and n-octanoyl. For parts of the range "Ci-8-acyl" all subgroups thereof are contemplated such as Ci.7-acyl, Ci-6-acyl, Ci-5-acyl, Ci^-acyl, C2-g-acyl, C2-7-acyl, C2.6-acyl, C2-5-acyl, C3-7-acyl, C4-6-acyl, etc.
[0325] C2-8-alkenyl in the compound of formula (I) according to the present application may be .a straight or branched acyl group containing 2-8 carbon atoms. Exemplary alkenyl groups include vinyl, 1-propenyl, 2-propenyl, isopropenyl, 1 -butenyl, 2-butenyl, 1-pentenyl, 2-pentenyl, 1-hexenyl, 2-hexenyl, 1-heptenyl, and 1-octenyl. For parts of the range "C2-8-alkenyl" all subgroups thereof are contemplated such as C2-7-alkenyl, C2.6-alkenyl, C2.5-alkenyl, C2-4-aIkenyl, C3-8-alkenyl, C3-7-alkenyl, C3-6-alkenyl, C3-5-alkenyl, C4-7-alkenyl, C5-6-alkenyl, etc.
[0326] C3-io-cycloalkyl in the compound of formula (I) according to the present application may be an optionally substituted monocyclic, bicyclic or tricyclic alkyl group containing between 3-10 carbon atoms. Exemplary cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, bicyclo[2.2.1]hept-2-yl, tricyclo[3.3.1.0~3,7~]non-3-yl, (lR,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1. l]hept-3-yl, (lS,2S,3S,5R)-2,6,6-trimethylbicyclo[3.1.1 ]hept-3-yl, 1 -adamantyl, noradamantyl, and 2,2,3, 3-tetramethylcyclopropyl. For parts of the range "C3-]0-cycloalkyl" all subgroups thereof are contemplated such as C3-9-cycloalkyl, C3-8-cycloalkyl, C3-7-cycloalkyl, C3-6-cycloalkyl, C3-5-cycloaikyl, C4-i0-cycloalkyl, C5-]0-cycloalkyl, C6-]0-cycloalkyl, C7-io-cycloalkyl, Cs-p-cycloalkyl, etc. In addition, the cycloalkyl moiety may optionally be substituted with one or more oxo groups.
[0327] C3-io-cycloalkenyl in the compound of formula (I) according to the present application may be an optionally alkyl substituted cyclic, bicyclic or tricyclic alkenyl group containing totally 3-10 carbon atoms. Exemplary cycloalkenyl groups include cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, cyclononenyl, cyclodecenyl, and bicyclo[2.2.1]hept-5-en-2-yl. For parts of the range "C3-io-cycloalkenyl" . all subgroups thereof are contemplated such as C3-9-cycloalkenyl, C3-g-cycloalkenyl, C3-7-cycloalkenyl, C3-6-cycloalkenyl, C3.5-cycloalkenyl, C4-io-cycloalkenyl, Cs.jo-cycloalkenyl, C6- lo-cycloalkenyl, C7-io-cycloalken}'l, Cg-g-cycloalkenyl, etc. In addition, the cycloalkenyl moiety may optionally be substituted with one or more oxo groups. [0328J The term "halogen" or "halo" in the present description is intended to include fluorine, chlorine, bromine and iodine.
[0329] The term "sulfanyl" in the present description means a rhio group.
[0330] The term "-hetero(Ci-Cg)alkyl" refers to a moiety wherein a hetero atom, selected from optionally substituted nitrogen, sulfur and Oxygen, is the point of attachment to the core molecule and is attached to a Ci-C8 alkyl chain.
[0331] The term "cyclic amide spiro ring" refers to compounds where the substituents at the 5-position of the thiazol none or the oxazolone ring combine together to form a cyclic ring having a -NR10C(O)- therein. An example of such a moiety is shown in the example below:
[0333] With the expression "mono- or di-substituted" is meant in the present description that the functionalities in question may be substituted with independently Cj.g-acyl, C2-8-alkenyl, C1-8-(cyclo)alkyl, aryl, pyridylmethyl, or heterocyclic rings e.g. azetidine, pyrrolidine, piperidine, piperazine, morpholine and thiomorpholine, which heterocyclic rings optionally may be substituted with Ci-8-alkyl. With the expression "optionally mono- or disubstituted" is meant in the present description that the functionalities in question may also be substituted with independently hydrogen.
[0334] When two of the above-mentioned terms are used together, it is intended that the latter group is substituted by the former. For example, Cs-io-cycloalkyl-Ci.g-alkyl means a 36 Ci-g-alkyl group that is substituted by a C3.10-cycloa.kyl group. Likewise, a Ci-8-haloalkyl means a Ci.g-alkyl group that is substituted by a halogen atom.
[0335] Metabolites of the compounds of Formula (I), (II), (III) and (IV) can take on many forms and the present invention encompasses the metabolites of the compounds as well as the parent compound.
[0336] As used herein, the term "prodrug" means a derivative of a compound that can hydrolyze, oxidize, or otherwise react under biological conditions (in vitro or in vivo) to provide an active compound, particularly a benzamide derivative. Examples of prodrugs include, but are not limited tOj derivatives and metabolites of a benzamide derivative that include biohydrolyzable groups such as biohydrolyzable amides, biohydrolyzable esters, biohydrolyzable carbamates, biohydrolyzable carbonates, biohydrolyzable ureides, and biohydrolyzable phosphate analogues (e.g., monophosphate, diphosphate or triphosphate). Preferably, prodrugs of compounds with carboxyl functional groups are the lower alkyl esters of the carboxylic acid. The carboxylate esters are conveniently formed by esterifying any of the carboxylic acid moieties present on the molecule. Prodrugs can typically be prepared using well-known methods, such as those described by Burge 's Medicinal Chemistry and Drug Discovery 6th ed. (Donald J. Abraham ed., 2001, Wiley) and Design and Application of Prodrugs (H. Bundgaard ed., 1985, Harwood Academic Publishers Gmfh).
[0337] "Tautomer" is one of two or more structural isomers that exist in equilibrium and are readily converted from one isomeric form to another, in the present case, tautoniers of the structures below are encompassed by the present invention.
[0339] As used herein, "hydrate" is a form of a compound of Formula (I), (II), (III), or (IV) where water molecules are combined in a definite ratio as an integral part of the crystal structure of the compound. 37
[0340] As used herein,"solvate" is a form of of a compound of Formula (I), (II), (ITS), or (IV) where solvent molecules are combined in a definite ratio as an integral part of the crystal structure of the compound.
[0341] Depending on its structure, the phrase "pharmaceutically acceptable salt," as used herein, refers to a pharmaceutically acceptable organic or inorganic acid or base salt of a benzamide derivative.. Representative pharmaceutically acceptable salts include, e.g., alkali metal salts, alkali earth salts, ammonium salts, water-soluble and water-insoluble salts, such as the acetate, amsonate (4,4-diaminostilbene-2, 2 -disulfonate), benzenesulfonate, benzonate, bicarbonate, bisulfate, bitartrate, borate, bromide, butyrate, calcium, calcium edetate, camsylate, carbonate, chloride, citrate, clavulariate, dihydrochloride, edetate, edisylate, estolate, esylate, fiunarate, gluceptate, gluconate, glutamate, glycollylarsanilate, hexafluorophosphate, hexylresorcinate, hydrabamine, hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isothionate, lactate, lactobionate, laurate, malate, maleate, mandelate, mesylate, methylbromide, methylnitrate, methylsulfate, mucate, napsylate, nitrate, N-methylglucamine ammonium salt, 3-hydroxy-2-naphthoate, oleate, oxalate, palmitate, pamoate (1 , l-methene-bis-2-hydroxy-3-naphthoate, einbonate), pantothenate, phosphate/diphosphate, picrate, polygalacturonate, propionate, p-toluenesulfonate, salicylate, stearate, subacetate, succinate, sulfate, sulfosaliculate, suramate, tannate, tartrate, teoclate, tosylate, triethiodide, and valerate salts. Furthermore, a pharmaceutically acceptable salt can * ■> . · ·, , , T ■. :— -i_ ... _i . „»;«.ii„ acceptable salt can have multiple counterions. Hence, a pharmaceutically acceptable salt can have one or more charged atoms and/or one or more counterions.
[0342] As used herein , the term "geometrical isomers" refers compounds that have the same molecular formula but the atoms are in different non-equivalent positions to one another.
[0343] As used herein, the term "optical isomers" refers to compounds with chiral atoms which have the ability to rotate plane polarized light, R/S configuration. The term optical isomer include enantiomers and diastereomers as well as compounds which can be distinguished one from the other by the designations of (D) and (L).
[0344] As used herein:
[0345] DCM means dichloromethane,
[0346] DEAD means diethyl azocarboxylate, 38
[0347] DMF means dimethylformamide,
[0348] EDCI means l -(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride,
[0349] Ether means diethyl ether,
[0350] EtOAc means ethylacetate,
[0351] HOBt means 1 -hydroxybenzotriazole,
[0352] HPLC means high-performance liquid chromatography,
[0353] LC means liquid chromatography,
[0354] MeCN means acetonitrile,
[0355] DPPA means diphenylphosphoryl azide, .
[0356] RT means room temperature,
[0357] SM means starting material,
[0358] TEA means triethylamine, and
[0359] THF means tetrahydrofuran.
[0360] Combinations of substituents and variables envisioned by this invention are only those that result in the formation of stable compounds. The term "stable", as used herein, refers to compounds which possess stability sufficient to allow manufacture and which maintains the integrity of the compound for a sufficient period of time to be useful for the purposes detailed herein (e.g., therapeutic administration to a subject for the treatment of disease, 1 1-β-HSDl inhibition, Ι Ι-β-HSDl-mediated disease).
[0361] The term "prodrug forms" in the present description means a pharmacologically acceptable derivative, such as an ester or an amide, which derivative is biotransformed in the body to form the active drug (see Goodman. and Gilman's, The Pharmacological basis of Therapeutics, 8lh ed„ McGraw-Hill, Int. Ed. 1992, "Biotransformation of Drugs, p. 13-15). [03 2] "Pharmaceutically acceptable" means in the present description being useful in preparing a pharmaceutical composition that is generally safe, non-toxic and neither biologically nor otherwise undesirable and includes being useful for veterinary use as well as human pharmaceutical use.
[0363] "Pharmaceutically acceptable salts" mean in the present description salts which are pharmaceutically acceptable, as defined above, and which possess the desired pharmacological activity. Such salts include acid addition salts formed with organic and inorganic acids, such as hydrogen chloride, hydrogen bromide, hydrogen iodide, sulfuric 39 acid, phosphoric acid, acetic acid, glycolic acid, maleic acid, malonic acid, oxalic acid, methanesulfonic acid, trifluoroacetic acid, fumaric acid, succinic acid, tartaric acid, citric acid, benzoic acid, ascorbic acid and the like. Base addition salts may be formed with organic and inorganic bases, such as sodium, ammonia, potassium, calcium, ethanolamine, diethanolamine, N-methylglucamine, choline and the like. Included in the invention are pharmaceutically acceptable salts or compounds of any of the formulae herein.
[0364] Pharmaceutical compositions according to the present invention contain a pharmaceutically acceptable carrier together with at least one of the compounds comprising the formula (I) as described herein above, dissolved or dispersed therein as an active, antimicrobial, ingredient. In a preferred embodiment, the therapeutic composition is not immunogenic when administered to a human patient for therapeutic purposes, unless that purpose is to induce an immune response.
[0365] The preparation of a pharmacological composition that contains active ingredients dissolved or dispersed therein is well understood in the art. Typically such compositions are prepared as sterile injectables either as liquid solutions or suspensions, aqueous or non-aqueous, however, solid forms suitable for solution, or siispensions, in liquid prior to use can also be prepared. The preparation can also be emulsified.
[0366] The active ingredient may be mixed with, excipients, which are pharmaceutically acceptable and compatible with the active ingredient and in amounts 1 1 - e— .— " 4,n«m«i4ii< m atltn e ΛΜ ΤΪΚΑ/Ι TI TMTI S ita le. p finiftTitR ate. for example, water, saline, dextrose, glycerol, ethanol or the like and combinations thereof. In addition, if desired, the composition may contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents and the like which enhance the effectiveness of the active ingredient. Adjuvants may also be present in the composition.
[0367] Pharmaceutically acceptable carriers are well known in the art. Exemplary of liquid carriers are sterile aqueous solutions that contain no materials in addition to the active ingredients and water, or contain a buffer such as sodium phosphate at physiological pH value, physiological saline or both, such as phosphate-buffered saline. Still further, aqueous carriers can contain more than one buffer salt, as well as salts such as sodium and potassium chlorides, dextrose, propylene glycol, polyethylene glycol and other solutes. 40
[0368] Liquid compositions can also contain liquid phases in addition to and to the exclusion of water. Exemplary of such additional liquid phases are glycerine, vegetable oils such as cottonseed oil, organic esters such as ethyl oleate, and water-oil emulsions.
[0369] The pharmaceutical composition according to one of the preferred embodiments of the present invention comprising compounds comprising the formula (I), may include pharmaceutically acceptable salts of that component therein as set out above. Pharmaceutically acceptable salts include the acid addition salts (formed with the free amino groups of the polypeptide) that are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic acid, tartaric acid, mandelic acid and the like. Salts formed with the free carboxyl groups can also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, 2-ethylaminoethahol, histidine, procaine and the like.
[0370] The preparations according to the preferred embodiments may be administered orally, topically, intraperitoneally, intraarticularly, intracranially, intradermally, intramuscularly, intraocularly, intrathecally, intravenously, subcutaneously. Other routes are known to those of ordinary skill in the art.
[0371] The orally administrable compositions according to the present invention may be in the form of tablets, capsules, powders, granules, lozenges, liquid or gel preparations, such as oral, topical or sterile parenteral solutions or suspensions. Tablets and capsules for oral administration may be in unit dose presentation form and may contain conventional excipients such as binding agents, for example syrup, acacia, gelatin, sorbitol, traganath or polyvinylpyrrolidone; fillers e.g. lactose, sugar, maize-starch, calcium phosphate, calcium hydrogen phosphate, sodium starch glycolate, sorbitol or glycine; tabletting lubricant e.g. magnesium stearate, talc, polyethylene glycol or silicon dioxide (optionally colloidal); disintegrants e.g. potato starch, or acceptable wetting agents such as sodium lauryl sulfate. The tablets may be coated according to methods well known in normal pharmaceutical practice. Oral liquid preparations may be in the form of e.g. aqueous or oily suspensions; solutions, emulsions, syrups or elixirs or may be presented as a dry product for reconstiturion with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents^ e.g. sorbitol, syrup, methyl cellulose (optionally macrocrystalline), glucose syrup, gelatin hydrogenated edible fats; 41 emulsifying agents e.g. lecithin, sorbitan monooleate or acacia, non-aqueous vehicles (which may include edible oils), e.g. almond oil, fractionated coconut oil, oily esters such as glycerine, propylene glycol, or ethyl alcohol; preservatives e.g. methyl or propyl p-hydroxybenzoate or sorbic acid, and if desired conventional flavouring or colouring agents.
[0372] "An effective amount" refers to an amount of a compound which confers a therapeutic effect on the treated subject. The therapeutic effect may be objective (i.e., measurable by some test or marker) or subjective (i.e., subject gives an indication of or feels an effect). A pharmaceutical composition according to the present invention, may comprise typically an amount of at least 0.1 weight percent of compound comprising the formula (I) per weight of total therapeutic composition. A weight percent is a ratio by weight of total composition. Thus, for example, 0.1 weight percent is 0.1 grams of compound comprising the formula (I) per 100 grams of total composition. A suitable daily oral dose for a mammal, preferably a human being, may vary widely depending on the condition of the patient.
However a dose of compound comprising the formula (I) of about 0.1 to 300 mg/kg body weight may be appropriate.
[0373] The compositions according to the present invention may also be used veterinarily and thus they may comprise a veterinarily acceptable excipient or carrier. The compounds and compositions may be thus administered to animals, e.g., cats, dogs, or horses, in treatment methods. labelled, may be used as a diagnostic agent.
[0375] This invention relates to methods of making compounds of any of the formulae herein comprising reacting any one or more of the compounds of the formulae delineated herein, including any processes delineated herein. The compounds of formula (I) above may be prepared by, or in analogy with, conventional methods, and especially according to or in analogy with the following methods. Further, the pharmacology in-vitro was studied using the following reagents and methods.
[0376] The chemicals used in the synthetic routes delineated herein may include, for example, solvents, reagents, catalysts, and protecting group and deprotecting group reagents. The methods described above may also additionally include steps, either before or after the steps described specifically herein, to add or remove suitable protecting groups in order to ultimately allow synthesis of the compounds. In addition, various synthetic steps may be 42 performed in an alternate sequence or order to give the desired compounds. Synthetic chemistry transformations and protecting group methodologies (protection and deprotection) useful in synthesizing applicable compounds are known in the art and include, for example, those described in R. Larock, Comprehensive Organic Transformations, VCH Publishers (1989); T.W. Greene and P.G.M. Wuts, Protective Groups in Organic Synthesis, 3rd Ed., John Wiley and Sons (1999); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis, John Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995) and subsequent editions thereof.
[0377] All publications mentioned herein are hereby incorporated by reference. By the expression "comprising" means "including but not limited to." Thus, other non-mentioned substances, additives or carriers may be present.
[0378] The invention will now be described in reference to the following Examples. These Examples are not to be regarded as limiting the scope of the present invention, but shall only serve in an illustrative manner.
* * * * EXAMPLES BIOLOGICAL EXAMPLES Scintillation Proximity Assay
[0379] [1, 2(n) - 3H]-cortisone was purchased from Amersham Pharmacia Biotech. Anti-cortisol monoclonal mouse antibody, clone 6D6.7 was obtained from Immunotech and Scintillation proximity assay (SPA) beads coated with monoclonal antimouse antibodies were from Amersham Pharmacia Biotech. NADPH, tetrasodium salt was from Calbiochem and glucose-6-phosphate (G-6-P) was supplied by Sigma. The human 11-β-hydroxysteroid dehydrogenase type-1 enzyme (Ι Ι-β-HSDi) was expressed in Pichia pastoris. 18-β-glycyrrhetinic acid (GA) was obtained from Sigma. The serial dilutions of the compounds were performed on a Tecan Genesis RSP 150. Compounds to be tested were dissolved in DMSO (1 mM) and diluted in 50 mM Tris-HCl, pH 7.2 containing 1 mM EDTA.
[0380] The multiplication of plates was done on a WallacQuadra. The amount of the product [3H]-cortisol, bound to the beads was determined in a Packard, Top Count microplate liquid scintillation counter. 43
[0381] The 11 -β-HSDi enzyme assay was carried out in 96 well microtiter plates (Packard, Optiplate) in a total well volume of 220 μΐ, and contained 30 mM Tris-HCl, pH 7.2 with 1 mM EDTA, a substrate mixture tritiated Cortisone/NADPH (175 nM / 181 μΜ), G-6- P (1 mM) and inhibitors in serial dilutions (9 to 0.15 μΜ). Reactions were initiated by the addition of human 1 Ι-β-HSDi, either as Pichia pastoris cell homogenate or microsomes prepared from Pichia pastoris (the final amount of enzyme used was varied between 0.057 to 0.11 mg/mL). Following mixing, the plates were shaken for 30 to 45 minutes at room temperature. The reactions were tennmated with 10 μΐ, 1 mM GA stop solution. Monoclonal mouse antibody was then added (10 ih of 4 μΜ) followed by 100 μΐ, of SPA beads (suspended according to the manufacturers instructions). Appropriate controls were set up by omitting the ΙΙ-β-HSDi to obtain the non-specific binding (NSB) value.
[0382] The plates were covered with plastic film and incubated on a shaker for 30 minutes, at room temperature, before counting. The amount of [3H]-cortisol, bound to the beads was determined in a microplate liquid scintillation counter. The calculation of the Κ,- values for the inhibitors was performed by use of Activity Base. The ¾ value is calculated from IC50 arid the Km value is calculated using the Cheng Prushoff equation (with reversible inhibition that follows the Michaelis-Menten equation): Κ,· = IC5o(l+[S]/Km) [Cheng, Y.C.; Prushoff, W.H. Biochem. Pharmacol. 1973, 22, 3099-3108]. The ICS0 is measured experimentally in an assay wherein the decrease of the turnover of cortisone to Cortisol is UCpeuueui UU LUC mmuiuuu ijuiouucu ua. ta i i iit, AVI vaiuui ui u.v_. unijjuuijuo ui the present invention for the 11-β-HSDl enzyme lie typically between about 10 nM and about 10 μΜ. Below follow some Ki examples according to the present invention.
Cloning, Expression and Purification of ΙΙβ-HSDl
[0383] The expression and purification of the murine enzyme is described by J. Zhang, et al. Biochemistry, 44, 2005, pp 6948-57. The expression and purification of the human enzyme is similar to that of the murine sequence. 44 Enzyme Assay:
[0384] The IC50 and Ki of the compounds are determined by the following method
[0385] 1. Prepare an Assay Buffer, (pH 7.2, 50 mM Tris-HCL, 1 mM EDTA) fresh each week.
[0386] 2. Prepare the following solutions:
[0387] NADPH (Sigma, 200 μΜ) [03381 3H:-Cortisone(Amersham Biosciences, 45 Ci/mmol, 200 nM)
[0389] Enzyme Prep (20 nM for human, 10 nM for mouse)
[0390] Cortisol Antibody (East Coast Biologicals, (1 :50 dilution) [0391 ] " Anti-mouse SPA beads (Amersham Biosciences, 15 mg/ml)
[0392] 1 Sp-Glycyrrhetinic acid ("GA")(Aldrich, 1 μΜ)
[0393] Compound Stock Solution(l OmM in D SO), serially diluted in assay buffer. Each compound is tested at six different concentrations usually (10 μΜ to 0.1 nM). All of the solutions and dilutions are made in the Assay Buffer.
[0394] 3. Assay is run using white/white, 96-well assay plates (Corning) in a total volume of 100 μΐ,.
[0395] 4. Into each well of a 96-well plate is added Assay Buffer (30 \xL), compound ( θ ) NADPH (10 JJL), and 3H-cortisone (10 μΙ_).
[0396] 5. Initiate reaction by adding 40 μΐ, of HSD-1 enzyme prep to the wells.
[0397] 6. The plate is covered with tape and incubated on an orbital shaker for 1 h at RT.
[0398] 7. After 1 h, the tape is removed and anti-cortisol antibody (10 μΐ,), GA solution (10 μΐ,), and SPA bead preparation (100 μΐ.) is added.
[0399] 8. The plate is incubated (30 min) on an orbital shaker at RT.
[0400] 9. The counts are read on a TqpCount NXT reader.
[0401] 10. A dose-reponse curve is first plotted using the Graphpad Prism software, to generate the IC50 values.
[0402] · With this IC50 value and the known Km value for the substrate and HSDl enzyme, an estimated Ki can be calculated with the Chen and Prusoff equation {Ki =TC50/ [1+ (substrate Km)]}. - . . 45
[0403] In addition to the above examples, the compounds of the present invention all show 1 Ιβ-HSDl enzyme activity (IC50) in the assays ranging from lOnM and 10 μΜ.
[0404] The following compounds exhibited activity in the Enzyme assay with IC50 values less than 20 nM:
[0405] 2-((3-chloro-2-methylphenyl)amino)-5-( 1 -methylethyl)- 1 ,3-thiazol-4(5H)-one;
[0406] 5-methyl-5-( yridin-4-yl)-2-(2-(trifluoromethyl)phenylamino)thiazol-4(5H) one; [040η 2-((2-chlorophenyl)amino)-5-methyl-5-phenyl-l,3-thiazol-4(5H)-one
[0408] (5S)-2-((2-chlorophenyl)amino)-5-methyl-5-phenyl-l,3-thiazol-4(5H)-one;
[0409] (5R)-2-((2-chlorophen)d)amino)-5-methyl-5-(l-methylethyl)-l)3-thiazol-4(5H)-one;
[0410] 2-((2-chlorophenyl)amino)-5-methyl-5-(l -methylethyl)- l,3-thiazol-4(5H)-one;
[0411] 2-((S)- 1 -cyclohexylethylamino)-5-isopropyl-5-methylthiazol-4(5H)-one;
[0412] (5S57R)-2-(cyclooctylamino)-7-(methyloxy)-l-thia-3-azaspiro[4.5]dec-2-en 4-one;
[0413] 2-((lSJ2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-((tetrahydro-2H pyran-4-yl)methyl)thiazol-4(5H)-one; one;
[0415] 2-(2-chlorophenylamino)-5-methyl-5-(tetrahydro-2H-pyran-4-yl)thiazol-4(5H)-one;
[0416] 2-((R)-l-(4-fluorophenyl)ethylamino)-5-isopropyl-5-methylthiazol-4(5H)-one;
[0417] 2-((255-difluorophenyl)amino)-5-(l-methylethyl)-l53-thiazol-4(5H)-one;
[0418] 2-(cyclohexylmethylaniino)-5-methyl-5-((S)-tetrahydrofuran-3-yl)thiazol-4(5H)-one;
[0419] 5-methyl-5-(l-methylethyl)-2-((2-(trifluoromethyl)phenyl)amino)-lJ3-thiazol-4(5H)-one;
[0420] 2-((lR,2R,4S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-propylthiazol-4(5H)-one; 46
[0421] 2-(o-toluidino)-5-cyclopentylthiazol-4(5H)-one ;
[0422] 2-((2-fluorophenyl)amino)-l-thia-3-azaspiro[4.4]non-2-en-4-one;
[0423] 2-((3-iluorotricyclo[3.3.1.1~3,7~]dec-l-yl)ammo)-5-methyl-5-(l-methylethyl)-l,3-thiazol-4(5H)-one;
[0424] (R)-5-isopropyl-5-methyl-2-((S)- 1 -phenylethylamino)thiazol-4(5H)-one;
[0425] 2-((2,6-dicmorophenyl)amino)-5-(l-methylethyl)-l ,3-thiazol-4(5H)-one;
[0426] 2-(cyclohexylmethylamino)-5-((S)-tetrahydrofuran-3-yl)thiazol-4(5H)-one;
[0427] 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-5-methyl-l,3-thiazol-4(5H)-one;
[0428] 2-(2-chlorophenylamino)-5-cyclopentylthiazol-4(5H)-one;
[0429] 2-(2-chlorophenylamino)-5-cyclohexylthiazol-4(5H)-one;
[0430] 2-((2-chlorop enyl)amino)-5-(l-methylethyl)-l,3-thiazol-4(5H)-one ;
[0431] 2-((S)-l-(4-iluorophenyl)ethylamino)-5-methyl-5-(pyridin-4-yl)thiazol-4(5H)-one;
[0432] 2-((S)-l-(2-fluorophenj4)ethylamino)-5-methyl-5-(pyridin-4-yl)thiazol-4(5H)-one;
[0433] 2-(2-fluorophenylamino)-5-((S)-tetrahydrofuran-3-yl)thiazol-4(5H)-one;
[0434] 2-((lR,2R,4S)-bicyclo[2.2. l]heptan-2-ylamino)-5-methyl-5-(2,2,2-trifluoroet yl)t iazol-4(5H)-one;
[0435] 5-ethyl-5-methyl-2-(tricyclo[3 ~3,7~]dec-l-ylamino)-l ,3-thiazol-4(5H)-one;
[0436] 2-(2-chlorophenylamino)-5-methyl-5-(pyridin-4-yl)thiazol-4(5H)-one;
[0437] 5-cyclopentyl-2-(2-fluorophenylamino)thiazol-4(5H)-one;
[0438] 5-cyclo exyl-2-(2-fluorophenylamino)thiazol-4(5H)-one;
[0439] 2-((R)-l-(2-fluorophenyl)ethylamino)-5-isopropyl-5-methylthiazol-4(5H)-one;
[0440] (R)-2-((S)-l-(2-fluorophenyl)ethylamino)-5-isopropyl-5-methylthiazoI-4(5H)-one; and 2-((2,4-dichlorophenyl)amino)-5-(l-methylethyl)-l,3-thiazol-4(5H)-one. 47 SYNTHESIS EXAMPLES General Reaction schemes Method A [0441 ] All commercial starting materials are used without any purification. [0442) If the appropriate a-bromocarboxylic acid or ester not is commercially availiable, the substances has been prepared in accordance to this method:
[0443] The 2-amino-carboxylic acid (1.0 eq.) was suspended in 2.0 M H2S04 (4 eq.), KBr (8 eq.) was added and the mixture was cooled in an ice-bath. NaN02 (1.3 eq.) dissolved in water was added slowly. The reaction mixture was stirred for 4 h at ice-bath, before allowed to reach room temperature. The reaction mixture was extracted with EtOAc. TI,„ -t cp i pri w r σζΠ, hp.frvre, crvnr.entrated in vacuum. This eave the crude product which was used in the next step without further purification (J. Org. Chem. 2002, 67 (11), 3595-3600; Xinhua Qian; Bin Zheng; Brian Burke; Manohar T. Saindane and David R. Kronenthal).
Methods and materials 104 4) ! jj nucjear magnetic resonance ( MR) and 13C NMR were recorded on a Bruker PMR 500 spectrometer at 500.1 MHz and 125.1 MHz, respectively or on a JEOL eclipse 270 spectrometer at 270.0 MHz and 67.5 MHz, respectively. All spectra were recorded using residual solvent or tetramethylsilane (TMS) as internal standard. IR spectra were recorded on a Perkin-Elmer Spectrum 1000 FT-IR spectrometer. Electrospray mass spectrometry (MS) was obtained using an Agilent MSD mass spectrometer. Accurate mass 48 measurements were performed on a Micromass LCT dual probe. Elemental analyses were performed on a Vario El instrument or sent to Mikro Kemi in Uppsala.
[0445] Analytical HPLC were performed on Agilent 1100 system equipped with System A: ACE 3 (C8, 50x3.0mm) or System B: YMC ODS-AQ, (33x3.0 mm) using the eluent system: water/0.1 %TFA and CH3CN, lmL/min, with a gradient time of 3 min.
[0446] Preparative HPLC was performed on a Gilson system equipped with System A: ACE 5 C8 column (50x20mm) gradient time 5 min, system B: YMC ODS-AQ (150x30mm) gradient time 8.5 min or system C: YMC ODS-AQ (50x20mm) gradient time 5 min using the eluent system: water/0.1%TFA and CH3CN. Preparative flash chromatography was performed on Merck silica gel 60 (230-400 mesh).
Synthetic Methodolology
[0447] Method A or B was used depending if the isothiocyanate or of the corresponding amine was used. The amine or the isothiocyanate was purchased from either Maybridge Pic. or from Sigma- Aldrich Co.
METHOD A
[0448] 1.0 eq. of the appropriate isothiocyanate was stirred in 2 M ammonia in ethanol (5 eq.) for 18 h at RT. Evaporation in vacuo afforded the crude product, which crystallized upon addition of DCM. The crystals were collected on a filter and air-dried to afford the thiourea.
METHOD B
[0449] 1.0 eq. of the amine and ethoxycarbonylisothiocyanate (1.0 eq) were mixed in a test tube. A violently exothermic reaction resulted in a white paste. This was taken up in 5M KOH solution and stirred at 70°C for 2 hours at which point LC analysis indicated full hydrolysis of the intermediate. The mixture was cooled, diluted with water and extracted 3 times with chloroform. Subsequent preparative LC yielded the desired thiourea.
METHOD C
[0450] The thiourea (1.0 eq.) and the cc-bromoester / ct-bromoacid (1,0 eq.) was dissolved in acetone and heated to 60°C in a sealed tube for 15 - 72 hours. The solvent was 49 removed. And the product purified by crystallization from MeOH / preparative reverse-phase HPLC.
METHOD CI
[0451] The thiourea (1.0 eq.) and the a-bromoester / a-bromoacid (1.0 eq.) was mixed in water and heated in the microwave at 140 °C for 1 hour. The aqueous phase was extracted twice with DCM. The combined orgaic phases were evaporated and the obtained crude product was purified by preparative reverse-phase HPLC.
METHOD D
[0452] The thiourea (1.0 eq.) and the a-bromoester (1.0 eq.) was dissolved in 1 ,4-dioxane and heated to 100 °C in a sealed tube for 1-11 days. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC.
METHOD Dl
[0453] The thiourea (1.0 eq.) and the a-bromoester (1.0 eq.) was dissolved in THF and heated to 70°C in a sealed tube for 1 day. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC.
METHOD D2
[0454] The thiourea (1.0 eq.) and the a-bromoester (1.0 eq.) was dissolved in 2-propanol and heated to 95°C in a sealed tube for 3 days. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC.
METHOD D3
[0455] The thiourea (1.0 eq.) and the α-bromoester / a-bromoacid (1.0 eq.) was dissolved in MeCN and heated to 60°C in a sealed tube for 2 days. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC.
METHOD E
[0456] The amino acid (1 eq.) was suspended in 2.0 M Η280 , KBr (8 eq.) was added and the mixture was cooled in an ice-bath. NaN02 (1.3 eq.) dissolved in water was slowly added. The reaction mixture was stirred for 4 h while cooling was continued. The reaction mixture was then extracted with EtOAc, washed with brine and brine containing 50 Na2S203. The organic phase was concentrated in vacuum. The product was used in the next step without further purification.
METHOD F
[0457] The thiourea (1 eq.) and 3-bromo-2-coumarone (1 eq.) was dissolved in acetone and heated to 60 °C for 3 hours. Water was added. The obtained solid was collected. Recrystallised from water/MeCN. The solid was collected. The mother liquor was concentrated and the obtained solid was dried in vaccum to give the product.
METHOD G
[0458] The carbonate salt of guanidine (1 eq.) and the alpha hydroxy ester (1 eq.) was dissolved in EtOH and heated to reflux for 2-10 hours. The mixture was then poured in to ¾0 and left at S°C for 16 hours. The product was collected by filtration.
METHOD H
[0459] The amino-oxazolone (1 eq.) and the amine (3 eq.) was added to 4 ml EtOH and put in the microwave oven at 130°C for 30 min. The solvent was removed under vacuum and the products purified by preparative reverse-phase HPLC.
METHOD I
[0460] To an ice-cooled solution with 1 eq. of the thiourea in DCM was 3 eq. 5% NaOH (aq) and 2 eq. dibromobutyryl chloride added followed by a small amount of benzyltriethylammonium chloride. The reaction was allowed to reach rt and additional 5 eq. 5% NaOH (aq) was added. The DCM-layer was separated and washed twice with water, dried over MgS04, filtered and concentrated. The product was isolated by preparative reverse-phase HPLC.
METHOD J
[0461] The acid (1 eq.) was dissolved in SOCl2 and heated to 60°C for 2 hours. NBS (2 eq.), SOCl2 and 1 drop of HBr (aq) was added at r.t. The reaction was heated to reflux for 75 min. The solvent was removed under vacuum, CCU was added and this was filtered. CCI4 was removed under vacuum. The remaining oil was dissolved in EtOH and left for 16 hours at r.t. The solvent was then removed under vacuum. This gave the product as an a-bromoester. 51 EXAMPLES
[0462] Methods A-J were employed for preparing the compounds of Exampl as described below.
Example l-2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-l,3-tliiazol-4(5H)-one
[0463] Synthesis was performed from N-bicyclo[2.2. l]hept-2-ylthiourea and ethyl 2-bromoisovalerate according to Method C. 104641 Ή NMR (400 MHz, DMSO-^) δ ppm 0.79 (m, 3 H) 0.97 (m, 3 H) 1.10 (m, 3 H) 1.45 (m, 4 H) 1.69 (m, 1 H) 2.22 (m, 2 H) 2.36 (m, 1 H) 3.74 (m, 1 H) 4.37 (m, 1 H) 9.56 (s, 1 H). MS (ESI+) for C13H20N2OS m/z 253 (M+H)+.
Example 2-2-(bicyclo[2.2.1]hept-2-ylamino)-5-ethyI-l,3-thiazol-4(5H)-one
[0465] Synthesis was performed from N-bicyclo[2.2.1 ]hept-2-ylthiourea and 104661 Ή NMR (400 MHz, DMSO-J6) δ ppm 0.90 (m, 3 H) 1.03-1.23 (m, 3 H) 1.35-1.56 (m, 4 H) 1.65-1.84 (m, 2 H) 1.98 (m, 1 H) 2.24 (m, 2 H) 3.75 (m, 1 H) 4.22-4.40 (m, 1 H) 9.84 (s, 1 H). MS (ESI+) for C12H18N2OS m/z 239 (M+H)+.
Example 3-2-(bicycIo[2.2.1]hept-2-ylamino)-5-phenyl-l,3-thiazol-4(5H)-one
[0467] Synthesis was performed from N-bicyclo[2.2.1]hept-2-ylthiourea and methyl alpha-bromophenylacetate according to Method C. 52 104681 Ή NMR (400 MHz, DMSO-Jd) δ ppm 1.05-1.24 (m, 3 H).1.36-1 ,56 (m, 4 H) 1.66-1.80 (m, 1 H) 2.22-2.33 (m, 2 H) 3.78-3.90 (m, 1 H) 5.41 (s, 0.5 H) 5.43 (s, 0.5 H) 7.21 -7.41 (m, 5 H) 9.39 (d, J=6.35 Hz, 1 H). MS (ESI+) for C,6H,8N2OS m/z 2S7 (M+H)+.
Example 4-2-(cyclohexylamino)-5-ethyl-l,3-thiazol-4(5H)-one
[0469] Synthesis was performed from n-cyclohexylthiourea and ethyl 2-bromobutyrate according to Method C. Gave 201 mg (75%). ,04701 Ή NMR (400 MHz, OMSO-d6) δ ppm 0.91 (m, 3 H) 1.05-2.06 (m, 12 (m, 1 H) 4.36 (m, 1 H) 10.11 (s, 1 H). MS (ESI+) for Ci iHlgN2OS m/z 227 (M+H)+ Example 5-2-( icyclo [2.2.1 ] hept-2-yIamin o)-5,5-dimethyI-l ,3-th iazoI-4(5H)-on e
[0471] Synthesis was performed from N-bicyclo[2.2. l]hept-2-ylthiourea and Ethyl 2-bromoisobutyrate according to Method C. . 10 721 Ή NMR (400 MHz, OMSO-d6) δ ppm 1.05 - 1.21 (m, 3 H) 1.34 - 1.54 (m, 4 H) 1.48 (s, 2 H) 1.49 (s, 2 H) 1.50 (s, 1 H) 1.51 (s, 1 H) 1.67 - 1.74 (m, 1 H) 2.18 - 2.28 (m, 2 H) 3.20 (dd, J=7.69, 2.93 Hz, 0.25 H) 3.73 - 3;S2 (m, 0.75 H) 9.12 (d, J=6.59 Hz, 1 H). MS (ESI+) for C12HlgN2OS m z 239 (M+H)+ Example 6-5-Isopropyl-2-(tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l,3-thiazoI-4(5ii)-one
[0473] Synthesis was performed from N-tricyclo [3.3.1.0-3 ,7~]non-3 -ylthiourea and ethyl 2-bromo-3-methylbutanoate according to Method C. 741 Ή NMR (400 MHz, DMSO-
[0475] Synthesis was performed from N-tricyclo[3.3.1.0~3,7~]non-3-ylthiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D. 104761 1H NMR (400 MHz, DMSO-cf6) δ 1.45-1.57 (m, 4 H), 1.90-2.16 (m, 8 H), 2.22-2.27 (m, 2 H), 2.44-2.55 (m, 5 H, obscured by solvent signal), 9.24 (s, 1 H). MS (ESI+) for Ci5H20N2OS m/z 111 (M+H)+.
Example 8-2-(Tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l,3-thiazoI-4(5i¾-one
[0477] Synthesis was performed from N-tricyclo[3.3.1.0~3,7~]non-3-ylthiourea and ethyl bromoacetate according to Method Dl. 104781 1H NMR (400 MHz, DMSO-.f6) δ 1.45-1.61 (m, 4 H), 1.92-2.07 (m, 6 H), 2.23 (m, 1.7 H, major rotamer), 2.82 (m, 0.3 H, minor rotamer), 2.45 (t, J= 6.7 Hz, 0.85 H, major rotanier), 2.66 (t, J- 6.8 Hz, 0.15 H, minor rotamer), 3.83 (s, 1.7 H, major rotamer), 4.09 (s, Example 9-6-(Cyclooctylamiao)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
[0479] Synthesis was performed from N-cyclooctylthiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D2. 104801 Ή NMR (400 MHz, DMSO-if6) δ 1.45-1.79 (m, 14 H), 1.86-2.00 (m, 1 H), 2.05-2.17 (m, 1 H), 2.41-2.53 (m, 4 H, obscured by solvent signal), 4.01 (m, 1 H), 9.09 (d, J = 7.5 Hz, 1 H). ,04811 13C NMR (100 MHz, DMSO-c/6) δ 16.31, 23.07, 24.97, 26.69, 30.88, 33.52, 54.69, 60.30, 175.09, 191.25. MS (ESI+) for Ci4H22N2OS m/z 267 (M+H)+. 54 Example 10-6-(CycloheptyIamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
[0482] Synthesis was performed from N-cycloheptylthiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D. 104831 Ή NMR (400 MHz, DMSO-d6) δ 1.35-1.65 (m, 10 H), 1.83-1.97 (m, 3 H), 2.05-2.17 (m, 1 H), 2.41-2.53 (m, 4 H, obscured by solvent signal), 3.96 (m, 1 H), 9.09 (d, J = 7.5 Hz, 1 H). MS (ESI+) for Ci3H20N2OS m/z 253 (M+H)+.
Example ll-6-(Bicyclo[2.2.1]hept-2-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
[0484] Synthesis was performed from N-bicyclo[2.2.1 ]hept-2-ylthiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D. 851 Ή NMR (400 MHz, DMSO-i6) δ 1.05-1.22 (m, 3 H), 1.33-1.49 (m, 4 H), 1.63-1.70 (m, 1 H), 1.86-2.00 (m, 1 H), 2.05-2.22 (m, 3 H), 2.42-2.53 (m, 4 H, obscured by solvent signal), 3.74 (m, 1 H), 8.98 (d, J= 7.5 Hz, 1 H). MS (ESI+) for C,3H18N2OS m/z 251 (M+H)+.
Example 12-6-[(2,2,3,3-Tetramethylcyclopropyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one
[0486] Synthesis was performed from N-(2,2,3 ,3-tetramethylcyclopropyl)thiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D. 871 1H NMR (400 MHz, DMSO-ci6) δ 0.92 (s, 3 H), 0.94 (s, 3 H), 1.06 (s, 3 H), 1.08 (s, 3 H), 1.88-2.00 (m, 1 H), 2.01 (s, 1 H), 2.06-2.17 (m, 1 H), 2:40-2.54 (m, 4 H, obscured by solvent signal), 8.78 (s br., 1 H). MS (ESI+) for C13H20N2OS m/z 253 (M+H)+. 55 Example 13-6-[(2-Methylphenyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-oae
[0488] Synthesis was performed from N-(2-methylphenyl)thiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D. 104891 Ή MR (400 MHz, DMSO--f6) δ 1.89 (m, 1 H), 2.04-2.13 (m, 1 H), 2.08 (s, 3 H), 2.39-2.48 (m3 2 H), 2.56-2.66 (m, 2 H), 6.81 (d, J= 7.6 Hz, 1 H), 7.03 (m, 1 H), 7.14 (m, 1 H), 7.20 (d, J= 7.4 Hz, 1 H), 11.67 (s br., 1 H). MS (ESI+) for C13H,4N2OS m/z 247 (M+H)+.
Example 14-2-[(cyclohexylmethyI)amino]-5,5-d{methyI-l,3-thiazol-4(5H)-oae
[0490] Synthesis was performed from N-(cyclohexylmethyl)thiourea bromoisobutyrate according to Method C. 104911 'H NMR (270 MHz, DMSO-^) 5 ppm 0.81 - 1.04 (m, 2 H) 1.03 - 1.32 (m, 3 H) 1 _n - 1 (m fi m 1 - 1 .78 (m. 6 m 3.18 - 3.32 fm. 2 Ή.) 9.28 is. 1 HI MS iEST+) for C12H20N2OS m/z 242 (M+H)+.
Example 15-2-[(2-fluorophenyl)amino]-5-isopropyl-l,3-thiazol-4(5H)-one
[0492] Synthesis was performed from N-(2-fluorophenyl)thiourea and Ethyl 2-bromo-2-methylbutyrate according to Method C. 104931 1H NMR (270 MHz, OMSO-d6) δ ppm 0.79 - 0.98 (m, 6 H) 2.29 - 2.44 (m, 1 H) 4.48 (d, J=3.59 Hz, 1 H) 6.91 - 7.40 (m, 4 H). MS (ESI+) for CnHnF^OSw/z 253 (M+H)+. 56 Example 16-2-[(cycIohexyImethyI)ammo]-5-(2-hydroxyphenyl)-l,3-thiazoI-4(5H)-one
[0494] Synthesis was performed from N-(cyclohexylmethyl)thiourea and 3-bromo- 2-coumarone according to Method F. 1049S1 Ή NMR (400 MHz, CHLOROFORM-D) δ ppm 0.80-1.00 (m, 2H) 1.05-1.27 (m, 3H) 1.55-1.81 (m, 6H) 3.24-3.34 (m, 2H), 5.42 (s, 1H) 6.73-6.81 (m, 2H) 7.02-7.14 (m,2H) 9.19 (br.s, 1 H, N-H) 9.81 (br.s, 1H, N-H). MS (ESI+) for C16H20N2O2S m/z 305 (M+H)+.
Example 17-(5S)-2-(c cloheptylamino)-5-methyl-l,3-thiazoI-4(5H)-one
[0496] Synthesis was performed from N-cycloheptylthiourea and (2S)-2- bromopropanoic acid according to Method C. 104971 Ή NMR (400 MHz, CHLOROFORM-D) δ ppm 1.35-1.70 (m, 12H) 1.45 (d, J = 7.3 Hz, 3H) 1.72-2.00 (m, 1H) 3.90-4.03 (m, 1H). MS (ESI+) for C, ,H,sN2OS m/z 221 (M+H)+.
Example 18-(5R)-2-(cycloheptj'lammo)-5-methyI-l,3-thiazol-4(5H)-one
[0498] Synthesis was performed from N-cycloheptylthiourea and (2R)-2- bromopropanoic acid according to Method C. 57 91 Ή NMR (400 MHz, CHLOROFORM-D) δ ppm 1.36-1.70 (m, 12H) 1.45 (d, J = 7.5 Hz, 3H) 1.82-1.96 (m, IH) 3.93-4.02 (m, IH). MS (ESI+) for CnH,8N2OS m/z 221 (M+H)+.
Example 19-2-(cy cloh eptylamin o)-5-ethyl-l ,3-thiazol-4(5H)-one
[0500] Synthesis was performed from N-cycloheptylthiourea and 2-bromobutyric acid according to Method C. 105011 Ή NMR (270 MHz, METHANOL-^) δ ppm 0.90 - 1.06 (m, 3 H) 1.40 - 2.17 (m, 14 H) 4.26 (dd, J=7.86, 4.02 Hz, 1 H) 4.52 - 4.68 (m, 1 H). MS (ESI+) for C12H20N2OS m/z 241 (M+H)+.
Example 20-2-(cycloheptylamino)-5-isopropyl-l,3-thiazol-4(5H)-one methylbutyrate according to Method C. 105031 Ή NMR (270 MHz, METHANOL-^) mixture of three different rotamers ~40%/30%/30% only the major; δ ppm 0.92 - 1.08 (m, 6 H) 1.43 - 2.16 (m, 12 H) 2.39 - 2.56 (m, 1 H) 3.98 - 4.20 (m, 1 H) 4.24 - 4.34 (m, 1 H). MS (ESI+) for C3H22N2OS m/z 255 (M+H)+.
Example 21-5-ier'-butyl-2-(cycloheptylamino)-l,3-thiazol-4(5J?)-one 58
[0504] Synthesis was performed from 2-amino-3,3-dimethy]butanoic acid and N- cycloheptylthiourea according to Method E and C. 105051 Ή NMR (270 MHz, METHANOL-^) δ ppm 0.S3 - 0.94 (m, 4.5 H) 0.98 - 1.12 (m, 4.5 H) 1.47 - 1.97 (m, 11 H) 2.36 - 2.58 (m, 1 H) 4.03 - 4.18 (m, 1 H) 4.34 - 4.42 (m, 1 H). MS (ESI+) for C]4H24N2OS m/z 269 (M+H)+.
Example 22-2-(cyclooctylamino)-5-ethyI-l,3-thiazol-4(5H)-one
[0506] Synthesis was performed from N-cyclooctyl-thiourea and 2-bromo-butyric acid according to Method CI. 105071 1H NMR (270 MHz, METHANOL-^) δ ppm 0.89 - 1.03 (m, 3 H) 1.43 - 1.99 (m, 15 H) 1.98 - 2.16 (m, 1 H) 4.21 - 4.32 (m, 1 H) 4.55 - 4.66 (m, 1 H). MS (ESI+) for C13H22N2OS m/z 255 (M+H)+.
Example 23-5-isopropyl-2-[(2-isopropylphenyl)amino]-l,3-thiazol-4(5H)-one
[0508] Synthesis was performed from N-(2-isopropylphenyl)thiourea and 2-bromo- 3-methylbutyric acid according to Method CI. 105091 Ή NMR (270 MHz, DMSC ¾ δ ppm 0.87 (dd, J=8.78, 6.80 Hz, 6 H) 1.12 - 1.17 (m, 6 H) 2.28 - 2.44 (m, 1 H) 2.93 - 3.09 (m, 1 H) 4.40 (d, J=3.46 Hz, 1 H) 6.83 (dd, J=7.24, 1.79 Hz, 1 H) 7.07 - 7.21 (m, 2 H) 7.26 - 7.36 (ra, 1 H).
[0510] MS (ESI+) for C,5H2oN2OS m/z 277 (M+H)+. 59 Example 24-5-ethyI-2- [(2-isopropylphenyl)amin o] -1 ,3-thiazol-4(5H)-on e [0511 ] Synthesis was performed from N-(2-isopropylphenyl)thiourea and 2-bromo-butyric acid according to Method CI. [05121 iH (270 MHz, DMSO- ) δ ppm 0.88 (t, J=7.30 Hz, 3 H) 1.14 (d, J=6.93 Hz, 6 H) 1.63 - 2.06 (m, 2 H) 2.93 - 3.11 (m, 1 H) 4.32 (dd, J=7.36, 4.27 Hz, 1 H) 6.75 - 6.92 (m, 1 H) 7.06 - 7.21 (m, 2 H) 7.24 - 7.42 (m, 1 H). MS (ESI+) for C,4H,8N2OS m/z 263 (M+H)+.
Example 25-2-I(2-cIiloroplienyl)amirio]-5-ethyl-l,3-thiazol-4(5H)-one
[0513] Synthesis was performed from N-(2-chlorophenyl)thiourea and 2-bromo-butyric acid according to Method CI. 105141 Ή NMR (270 MHz, METHANOL-^) δ ppm 1.01 - 1.23 (m, 3 H) 1.98 - 2.34 (m, 2 H) 4.58 - 4.72 (m, 1 Jd) 7.za - 4 ( , _> n I .D<* - / .uo , , lui CuHuClN2OS m/z 255 (M+H)+.
Example 26-5-ethyl-2-[(2-methylphenyl)amino]-l,3-thiazol-4(5H)-one
[0515] Synthesis was performed from N-(2-methylphenyl)thiourea and 2-bromo-butyric acid according to Method CI. 105161 Ή NMR (270 MHz, METHANOL-^) δ ppm 1.07 - 1.18 (m, J=7.36, 7.36 Hz, 3 H) 1.98 - 2.36 (m, 2 H) 2.11 - 2.13 (m, 3 H) 4.52 - 4.75 (m, 1 H) 7.12 (dd, J=20.54, 7.67 Hz, 1 H) 7.22 - 7.46 (m, 3 H). MS (ESI+) for Ci2Hi4N2OS m/z 235 (M+H)+. 60 Example 27-5-isopropyl-2-[(2,2,3s3-tetrainethylcyclopropyl)arnino]-l53-thiazoI-4(5H)-one
[0517] Synthesis was performed from N-(2,2,3,3-tetramethylcyclopropyl)thiourea and ethyl-2-bromoisovalerate according to Method C. 105181 ]H NMR (400 MHz, CDC13) δ ppm 0.99 (d, J=6.6 Hz, 3 H), 1.08 - 1.16 (m, 9 H), 1.20 (d, J=3.4 Hz, 6 H), 2.17 (s, 1 H), 2.59 - 2.72 (m, 1 H), 4.25 (d, J=3.9 Hz, 1 H). MS (ES+) m/z 255 (M+H ).
Example 28-2-(bicyclo[2.2.1]hept-2-ylamino)-5-(4-hydroxybenzyI)-l,3-thiazoI-4(5H)-one
[0519] Synthesis was performed from (25)-2-amino-3-(4-hydroxyphenyl)propanoic acid and N-bicyclo[2.2.1]hept-2-ylthiourea according to Method E and C. 105201 ]H NMR (270 MHz, DMSO-<¾ δ 1.11 (d, J=9.65 Hz, 3 H) 1.24-1.54 (m, 4 H) 1.56-1.76 (m, 1 H) 2.04-2.27 (m, 2 H) 2.61-2.84 (m, 1 H) 3.26 (dd, J=14.10, 3.96 Hz, 1 H) 3.70 (s, 1 H) 4.42-4.52 (obscured by HDO peak) (m, 1 H) 6.57-6.72 (m, 2 H) 6.92-7.08 (m, 2 H) 9.07 (d, J=6.19 Hz, 1 H) 105211 Ή NMR (270 MHz, METHANOL-^) δ 1.07-1.62 (m, 7 H) 1.67-1.88 (m, 1 H) 2.07-2.36 (m, 2 H) 2.92-3.11 (m, 1 H) 3.32-3.44 (partly obscured by MeOD peak) (m, 1 H) 3.64-3.76 (m, 1 H) 4.51-4.68 (m, 1 H) 6.62-6.76 (m, 2 H) 6.99-7.12 (m, 2 H). MS (ESI+) for Ci 7H20N2O2S m/z 317 (M+H)+ Example 29-5-[(cyclohexylmethyI)amino]-4^thia-6-azaspiro[2.4]hept-5-ea-7-one
[0522] Synthesis was performed from N-(cyclohexylmethyl)thiourea according to Method I. 61 T U 2005/ 18081 105231 Ή NMR (400 MHz, CHLOROFORM-D) δ ppm 0.94 - 1.07 (m, 2 H) 1.10 - 1.36 (m, 3 H) 1.49 - 1.54 (m, 2 H) 1.66 - 1.86 (m, 8 H) 3.19 (d, J=6.59 Hz, 2 H). MS m/z 239 (M+H)+ Example 30-2-(cycloheptylamino)-5-(3,4-dihydroxybenzyl)-l,3-thiazol-4(5H)-one
[0524] Synthesis was performed from (2iS)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid and N-cycIoheptylthiourea according to Method E and C. 105251 Ή NMR (500 MHz, Solvent) δ 1.43-1.57 (m, 6 H) 1.56-1.73 (m, 5 H) 1.84-2.01 (m, 2 H) 2.87 (dd, J=14.13, 9.42 Hz, 1 H) (1H hidden in MeOD peak) 3.97-4.06 (m, 1 H) 4.44-4,51 (m, 1 H) 6.52-6.57 (m, 1 H) 6.64-6.68 (m, 2 H). MS (ESI+) for C17H22N203S m/z 335 (M+H)+ Example 31-2-(cycloheptylamino)-5-(lH-imidazol-4-yImethyl)-l,3-thiazoI-4(5H)-one
[0526] Synthesis was performed from (2S)-2-ammo-3-(lH-imidazol-4-yl)propanoic acid and Y-cycloheptylthiourea according to Method E and C. |0S271 1H MR (270 MHz, METHANOL-^) δ 1.43-2.06 (m, 12 H) 3.33-3.56 (m, 2 H) 3.93-4.08 (m, 1 H) 4.57-4.69 (m, 1 H) 7.27-7.42 (m, 1 H) 8.76-8.87 (m, 1 H). MS (ESI+) for CI4H20N4OS m/z 293 (M+H)+ Example 32-2-(cycIoheptylamino)-5-isoburyl-l,3-thiazoI-4(5H)-one
[0528] Synthesis was performed from (25)-2-amino-4-methylpentanoic acid and N-cycloheptylthiourea according to Method E and C. 62 105291 Ή NMR (270 MHz, METHANOL-^) δ 0.91-1.04 (m, 6 H) 1.43-1.86 (m, 12 H) 1.92-2.12 (m, 3 H) 3.95-4.11 (m, 1 H) 4.29-4.48 (m, 1 H). MS (ESI+) for C14H24N2OS m/z 269 (M+H)+ Example 33-2-(cycloheptylammo)-5-(lH-mdol-3-ylmethyl)^l,3-thiazol-4(5H)-one : [0530] Synthesis was performed from (2£ -2-amino-3-(lH-indol-3-yl)propanoic acid and N-cycloheptylthiourea according to Method E and C. ί05311 Ή NMR (270 MHz, CHLOROFORM-D) δ 1.27 - 1.80 (m, 11 H) 1.84 - 1.99 (m, 1 H) 3.23 - 3.40 (m, 2 H) 3.76 (dd, J=15.09, 3.46 Hz, 1 H) 4.65 (d, J=9.15, 3.96 Hz, 1 H) 7.10 - 7.28 (m, 3 H) 7.40 (d, J=7.92 Hz, 1 H) 7.59 (d, J=7.92 Hz, 1 H) 8.26 (s, 1 H). MS (ESI+) for d 9H23N3OS m/z 342 (M+H)+ Example 34-2-(cycloheptylamino)-5-(4-hydroxybenzyI)-l,3-thiazol-4(5H)-one
[0532] Synthesis was performed from (2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid and N-cycloheptylthiourea according to Method E and C. 105331 1H NMR (270 MHz, METHANOL-^) δ ppm 1.37 - 2.07 (m, 12 H) 2.91 - 3.11 (m, 1 H) 3.32 - 3.43 (m, 1 H) 3.86 - 4.02 (m, 1 H) 4.48 - 4.66 (m, 1 H) 6.60 - 6.76 (m, 2 H) 6.99 - 7.11 (m, 2 H). MS (ESI+) for CnH22N202S m/z 319 (M+H)+. .
Example 35-(5i?)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-l,3-thiazol-4(5H)-one
[0534] Synthesis was performed from (2iS)-2-amino-3-cyclohexylpropan0ic acid and N-cycloheptylthiourea 'according to Method E and C. 63 105351 Ή NMR (270 MHz, CHLOROFORM-D) δ ppm 0.85 - 1.90 (m, 22 H) 1.93 -2:10 (m, 2 H) 2.14 - 2.30 (m, 1 H) 3.35 - 3.57 (m, 1 H) 4.23 (dd, J=l 1.32, 3.77 Hz, 1 H). MS (ESI+) for Ci7H28N2OS m/z 309 (M+H)+ Example 36-2-(cyclooctylamino)-5-(4-hydroxybenzyl)-l,3-thiazoI-4(5H)-one
[0536] Synthesis was performed from (2-S)-2-amino-3-(4-hydroxyphenyl)propanoic acid and N-cyclooctylthiourea according to Method E and C. Ή NMR (270 MHz, CHLOROFORM-D) δ ppm 1.41 - 1.95 (m, 14 H) 3.07 (dd, J=14.47, 9.65 Hz, 1 H) 3.43 - 3.59 (m, 2 H).4.46 (dd, J=9.65, 3.96 Hz, 1 H) 6.81 (d, J=8.41 Hz, 2 H) 7.08 (d, J=8.41 Hz, 2 H). MS (ESI+) for m/z 333 (M+H)+ Example 37-(5S)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-l,3-thiazol-4(5H)-one
[0538] Synthesis was performed from (2#)-2-amino-3-cyclohexylpropanoic acid and N-cycloheptylthiourea according to Method E and C. 2.11 (m, 2 H) 2.11 - 2.30 (m, 1 H) 3.34 - 3.60 (m, 1 H) 4.23 (dd, J=l 1.32, 3.77 Hz, 1 H) 8.81 (br.s, 1 H). MS (ESI+) for C]7H28N2OS m/z 309 (M+H)+ Example 38-[2-(cycIoheptylamino)-4-oxo-4,5-dihydro-l,3-thiazol-5-yl]acetonitrile
[0540] Synthesis was performed from (2_S)-2-amino-3-cyanopropanoic acid and N-cycloheptylthiourea according to Method E and C. [05411 Ή NMR (270 MHz, CHLOROFORM-D) δ ppm 1.36 - 2.14 (m, 12 H) 2.85 -3.11 (m, 1 H) 3.12 - 3.32 (m, 1 H) 3.43 - 3.58 (m, 1 H) 4.31 - 4.46 (m, 1 H). MS (ESI+) for Ci2Hi7N3OS m/z 252 (M+H)+ 64 Example 39-5-ethyl-2-[(3-methyiphenyl)amino]-l,3-thiazol-4(5H)-one
[0542] Commercial compound, SPECS.
[0543] MS (ESI+) for C12H]4N2OS m/z 235 (M+H)+
[0544] HPLC 99%, Rf=2.10 min (System A, 10-97% MeCN over 3 min).
[0545] HPLC 99%, Rr=l .58 min (System B, 10-97% MeCN over 3 min).
Example 40-2-(cycIoheptyIamino)-5-(pyridin-3-yImethyI)-l,3-tIiiazoI-4(5H)-one
[0546] Synthesis was performed from (2iS)-2-amino-3-pyridin-3-ylpropanoic acid and Nrcycloheptylthiourea according to Method E and C. 105471 iH iR ^270 ^ CHLOROFORM-D) δ ppm 1.39 - 1.84 (m, 9 H) 1.88 -2.06 (m, 2 H) 3.39 - 3.54 (m, 1 H) 3.64 (s, 2 H) 3.97 (s, 1 H) 4.75 (s, 1 H) 7.84 - 7.95 (m, 1 H) 8.34 (d, J=7.67 Hz, 1 H) 8.75 (d, J=5.07 Hz, 1 H) 9.10 (s, 1 H). MS (ESI+) for C16H2,N3OS m/z 304 (M+H)+ Example 41-5-Isopropyl-2-[(2-methylphenyl)amino]-l,3-thiazol-4(5-H)-one
[0548] Synthesis was performed from N-(2-methylphenyl)thiourea and ethyl 2-bromo-3-methylbutanoate according to Method C. 105491 'H NMR (400 MHz, DMSO-ii6) 5 0.84 (d, J= 6.6 Hz, 3 H), 0.88 (d, J= 7.0 Hz, 3 H), 2.10 (s, 3 H), 2.34 (m, 1 H), 4.32 (d, J= 3.4 Hz, 1 H), 6.83 (d, J= 7.8 Hz, 1 H), 7.03 (m, 1 H), 7.16 (m, 1 H), 7.21 (d, J= 7.6 Hz, 1 H). MS (ESI+) for C13H16N2OS m/z 249 (M+H)+. 65 Example 42-2-(Cyclooctylamino)-5,5-dimethyl-l,3-thiazol-4(5H)-one
[0550] Synthesis was performed from ethyl-2-bromo-2-methylpropanoate and N-cyclooctyltliiourea according to Method CI. 105511 Ή NMR (270 MHz, OUSO-d6) δ ppm 1.46 (s, 3H), 1.47 (s, 3H), 1.81-1.43 (m, 15H). MS (EI+) for C]3H22N2OS m/z 255 (M+H)+.
Example 43-2-(Cyclooctylamino)-5-isopropyl-l,3-thiazol-4(5H)-one
[0552] Synthesis was performed from 2-bromo-3-methylbutyric acid and N-cyclooctylthiourea according to Method CI . 105531 1H NMR (270 MHz, METHANOL-cW) Major isomer: δ ppm 0.85 (d, J=6.68 Hz, 3 H) 1.01 (d, J=6.93 Hz, 3 H) 1.44 - 1.91 (m, 14 H) 2.36 - 2.52 (m, 1 H) 3.98 - 4.12 (m, 1 H) 4.36 (d, J=3.71 Hz, 1 H). MS (EI+) for C,4H24N2OS m/z 269 (M+H)+.
Example 44-2-(Bicyclo [2.2.1 ] hept-2-ylamin o)-l -thia-3-azaspiro [4.5] dec-2-en-4-one 105541 Synthesis was performed from N-bicyclo[2.2. llhept-2-ylthiourea and methyl 1-bromocyclohexanecarboxylate according to Method D. 105551 Ή NMR (400 MHz, CDC13) δ 1.12-2.44 (m, 21 H), 3.34 (m, 1 H).
[0556] MS (ESI+) for Ci5H22N2OS m/z 279 (M+H)+.
Example 45-2-(Tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one
[0557] Synthesis was performed from N-tricyclo[3.3.1.0~3,7~]non-3-ylthiourea and methyl 1-bromocyclohexanecarboxylate according to Method D. 66 105581 Ή NMR (400 MHz, CDCI3) δ 1.24-2.19 (m, 20 H), 2.30 (m, 0.5 H, minor rotamer), 2.41 (m, 1.5 H, major rotamer), 2.53 (m, 0.25 H, minor rotamer), 2.75 (m, 0.75 H, major rotamer).
[0559] MS (ESI+) for Ci7H24N2OS m/z 305 (M+H)+.
Example 46-2-(Cycloheptylamino)-l-thia-3-azaspiro[4.5]dec-2-eii-4-one
[0560] Synthesis was performed from N-cycloheptylthiourea and methyl 1-bromocyclohexanecarboxylate according to Method D. 105611 Ή NMR (400 MHz, CDCI3) δ 1.24-2.14 (m, 23 H), 3.48 (m, 1
[0562] MS (ESI+) for d 5H24N2OS m/z 281 (M+H)+.
Example 47-2-(Cyclooctylamino)-l-thia-3-azaspiro(4.5]dec-2-en-4-one
[0563] Synthesis was performed from N-cyclooctylthiourea and methyl 1 -bromocyclohexanecarboxylate according to Method D. 1056 1 1H NMR (400 MHz, CDC13) 6 1.24-2.13 (m, 25 H), 3.55 (m, 1 H).
[0565] MS (ESI+) for C,6H26N2OS m/z 295 (M+H)+.
Example 48-2-{[l-(4-Chlorophenyl)cyclobutyl]amino}-5-isopropyl-l,3-thiazol-4(5i -one
[0566] Synthesis was performed from N-[l -(4-chlorophenyl)cyclobutyl]thiourea and ethyl 2-bromo-3-methylbutanoate according to Method D. 105671 Ή NMR (400 MHz, DMSO-rf6) δ 0.60 (d, J= 6.5 Hz, 0.75 H, minor rotamer), 0.68 (d, J= 6.6 Hz, 2.25 H, major rotamer), 0.82 (d, J= 6.8 Hz, 0.75 H, minor rotamer), 0.92 (d, J= 6.8 Hz, 2.25 H, major rotamer), 1.77-1.87 (m, 1 H), 1.93-2.03 (m, 1 H), 2.21-2.33 67 (m, 1 H), 2.42-2.65 (m, 4 H, obscured by solvent signal), 4.14 (d, J= 3.5 Hz, 0.25 H, minor rotamer), 0.68 (d, J= 3.7 Hz, 0.75 H, major rotamer), 7.38 (m, 3 H, major rotamer), 7.45 (m, 1 H, minor rotamer), 9.87 (s, 1 H).
[0568] MS (ESI+) for Ci6H] 9ClN2OS m/ 323 (M+H)+.
Example 49-6-{il-(4-Chlorophenyl)cyc]obutyl]amino}-5-thia-7-azaspiro[3.4]oct-6-en-8- one
[0569] Synthesis was performed from N-[l-(4-chlorophenyl)cyclobutyl]thiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D. 105701 1H NMR (400 MHz, OMSO-d6) δ 1.73-2.12 (m, 4 H), 2.32-2.60 (m, 8 H, obscured by solvent signal), 7.39 (m, 3.3 H, major rotamer), 7.44 (m, 0.7 H, minor rotamer), 9.83 (s, 1 H).
[0571] MS (ESI+) for Ci6H]7ClN2OS m/z 321 (M+H)+.
Example 50-2-(cycloheptylamino)-5,5-diethyl-l ,3-thiazol-4(5H)-one H
[0572] Synthesis was performed from N-cycloheptylthiourea and 2-ethylbutyric ' acid according to Method J and D. 105 31 1H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.89 - 1.01 (m, 6 H) 1.40 - 2.09 (m, 16 H) 3.44 - 3.55 (m, 1 H)
[0574] MS (ESI+) for C,4H24N2OS m/z 269 (M+H)+ Example 51-(5S)-5-isopropyl-2-{[(2S)-2-phenyIpropyI]amino}-l,3-thiazol-4(5H)-one 68
[0575] Synthesis was performed from N-[(2S)-2-phenylpropyl]thiourea and 2-bromo-3-methylbutyric acid according to Method D3- 105761 Ή NMR (270 MHz, DMSO-c¾ the major rotamer δ ppm 0.54 - 0.85 (m, 3 H) 0.84 - 1.08 (m, 3 H) 1.08 - 1.37 (m, 3 H) 2.18 - 2.43 (m, .1 H) 2.91 - 3.22 (m, 1 H) 3.27 - 3.47 (m, J=7.30 Hz, 1 H) 3.44 - 3.62 (m, 1 H) 4.18 - 4.37 (m, 1 H) 6.95 - 7.43 (m, 5 H) 9.26 (s, 1 H, N-H).
[0577] MS (ESI+) for C,5H20N2OS m/z 277 (M+H)+.
Example 52-(5R)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazo]-4(5H)-oue
[0578] Synthesis was performed from N-[(2S)-2-phenylpropyl]thiourea and 2-bromo-butyric acid according to Method D3. 105791 Ή NMR (270 MHz, DMSO-i¾ the major rotamer δ ppm 0.51 - 0.70 (m, 3 H) 1.10 - 1.36 (m, 3 H) 1.45 - 1.80 (m, 1 H) 3.11 - 3.34 (m, 1 H) 3.65 - 3.84 (m, 2 H) 3.80 - 4.07 (m, 1 H) 4.30 - 4.48 (m, 1 H) 7.10 - 7.41 (m, 5 H).
[0580] MS (ESI+) for C, H,8N2OS m/z 263 (M+H)+.
Example 53-(5S)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one
[0581] Synthesis was performed from N-[(2S)-2-phenylpropyl]thiourea and 2-bromo-butyric acid according to Method D3. 105821 Ή NMR (270 MHz, DMSO-<¾ the major rotamer δ ppm 0.73 - 0.97 (m, 3 H) 1.10 - 1.35 (m, 3 H) 1.53 - 1.82 (m, 1 H) 1.83 - 2.11 (m, 1 H) 2.92 - 3.13 (m, 1 H) 3.48 - 3.67 (m, 2 H) 4.10 - 4.32 (m, 1 H) 7.09 - 7.45 (m, 5 H) 9.27 (s, 1 H, N-H).
[0583] MS (ESI+) for C14Hi8N2OS m/z 263 (M+H)+. 69 Example 54-(5R)-5-isopropyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one
[0584] Synthesis was performed from N-[(2R)-2-phenylpropyl]thiourea and 2-bromo-3-methylbutyric acid according to Method D3. 10585] iH m/SR ^270 J^JJ^ rj SO-^ί) the major rotamer 5 ppm 0.50 - 0.80 (m, 3 H) 0.84 - 1.06 (m, 3 H) 1.09 - 1.32 (m, 3 H) 2.22 - 2.43 (m, 1 H) 2.91 - 3.19 (m, 1 H) 3.27 - 3.45 (m, 2 H) 4.14 - 4.38 (m, 1 H) 7.07 - 7:44 (m, 5 H) 9.25 (s, 1 H, N-H).
[0586] MS (ESI+) for C15H20N2OS m/z 211 (M+H)+.
Example 55-(5S)-5-isopropyI-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one
[0587] Synthesis was.performed from N-[(2R)-2-phenylpropyl]thiourea and 2- 105881 ¾ MR (270 MHz, DMSO-cfc) the major rotamer δ ppm 0.40 - 0.58 (m, J=6.68 Hz, 3 H) 0.71 - 0.87 (m, 3 H) 1.03 - 1.29 (m, 3 H) 2.11 - 2.24 (m, 1 H) 3.62 - 3.81 (m, 2 H) 3.83 - 4.03 (m, 1 H) 4.36 - 4.51 (m, 1 H) 7.10 - 7.41 (m, 5 H).
[0589] MS (ESI+) for C, 5H20N2OS m/z 111 (M+H)+.
Example 56-(5R)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazoI-4(5H)-one l 70
[0591] Synthesis was performed from N-[(2R)-2-phenylpropyl]thiourea and 2-bromo-butyric acid according to Method D3. 105921 Ή NMR (270 MHz, DMSO-<¾ the major rotamer δ ppm 0.75 - 0.97 (m, 3 H) 1.05 - 1.35 (m, 3 H) 1.58 - 1.82 (m, 1 H) 1.82 - 2.05 (m, 1 H) 2.92 - 3.17 (m, 1 H) 3.44 - 3.65 (m, 2 H) 4.12 - 4.36 (m, 1 H) 7.09 - 7.49 (m, 5 H) 9.26 (s, 1 H).
[0593] MS (ESI+) for CuHi8N2OS m/z 263 (M+H)+.
Example 57-(5S)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one
[0594] Synthesis was performed from N-[(2R)-2-phenylpropyl]thiourea and 2-bromo-butyric acid according to Method D3. 105951 1H NMR (270 MHz, DMSO-<¾ the major rotamer δ ppm 0.53 - 0.74 (m, J=7.30, 7.30 Hz, 3 H) 1.08 - 1.33 (m, 3 H) 1.43 - 1.63 (m, 1 H) 1.62 - 1.89 (m, 1 H) 3.13 -3.36 (m, 1 H) 3.66 - 3.86 (m, J=13.61, 7.17 Hz, 1 H) 3.83 - 4.04 (m, 1 H) 4.26 - 4.51 (m, j=4.95 Hz, 1 H) 7.09 - 7.44 (m, 5 H).
[0596] MS (ESI+) for C14H18N2OS m/z 263 (M+H)+.
Example 58-2-AniImo-5-isopropyl-l,3-thiazoI-4(5H)-one
[0597] Synthesis was performed from N-phenylthiourea and ethyl 2-bromo-3-rnethylbutanoate according to Method C. 105981 !H NMR (400 MHz, CHLOROFORM-D) δ ppm 1.00 (s, 6 H), 2.40 - 2.73 (m, 1 E), 4.04 - 4.34 (m, 1 H), 7.01 - 7.56 (m, 6 H); MS [M+H]+ m/z = 235. 71 Example 59-5-Isopropyl-2-[(2-morphoIin-4-ylethyI)amino]-l,3-thiazol-4(5H)-one
[0599] Synthesis was performed from N-(2-morpholin-4-ylethyl)thiourea and ethyl 2-bromo-3-methylbutanoate according to Method C. (0600) i H (400 Mft^ CHLOROFORM-D) δ ppm 0.70 - 1.25 (m, 8 H), 2.58 (s, 1 H), 2.78 - 4.09 (m, 10 H), 4.18 -.4.54 (m, 1 H); MS [M+H]+ m/z = 272.
Example 60-2-(Bicyclo[2.2.1]hept-2-ylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one Example 61-2-(Cycloheptylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one Example 62-2-(CycIooctylamino)-l-thia-3-azaspiro[4.4]aon-2-en-4-one Example 63-2-((2,2,3,3-Tetramethylcyclopropyl)amino]-l-thia-3-azaspiro[4.4]non-2-en-4-one [0601 ] Examples 60-63 were prepared using one of the methodologies described above.
[0602] Synthesis was performed from 2-amino-5-isopropyl-l ,3-oxazol-4(5H)-one and 2-Chlorobeiizylamine according to Method G + H. 106031 Ή NMR (400 MHz, DMSO-<¾ δ ppm 0.62 (d, J=6.84 Hz, 0.75 H) 0.82 (d, J=6.84 Hz, 2.25 H) 0.90 (d, J=6.96 Hz, 0.75 H) 0.99 (d, J=6.84 Hz, 2.25 H) 1.97 - 2.13 (m, 1 H) 4.41 - 4.50 (m, 0.5 H) 4.51 - 4.56 (m, 1.5 H) 4.59 (d, J=3.66 Hz, 0.25 H) 4.63 (d, J=3.66 Hz, 0.75 H) 7.30 - 7.41 (m, 3 H) 7.45 - 7.49 (m, 1 H) 9.30 (s, 1 H). MS (ESI+) for Ci3Hi5ClN202 m/z 267 (M+H)+ 72 Example 65-2-[(4-chlorobenzyl)amino]-5-isopropyl-l,3-oxazol-4(5H)-one
[0604] Synthesis was performed from 2-amino-5-isopropyl-l,3-oxazol-4(5H)-one and 4-Chlorobenzylamine according to Method G + H. 106051 1H N R (400 MHz, DMSO-c¾ δ ppm 0.63 (d, J=6.S4 Hz, 0.75 H) 0.80 (d, J=6.84 Hz, 2.25 H) 0.90 (d, J=6.96 Hz, 0.75 H) 0.98 (d, J=6.84 Hz, 2.25 H) 1.96 - 2.13 (m, 1 H) 4.37 - 4.41 (m, 0.5 H) 4.44 (d, J=6.10 Hz, 1.5 H) 4.58 (d, J=3.54 Hz, 0.25 H) 4.61 (d, J=3.78 Hz, 0.75 H) 7.27 - 7.34 (m, 2 H) 7.37 - 7.45 (m, 2 H) 9.28 (t, J=5.98 Hz, 0.75 H) 9.49 (s, 0.25 H).
[0606] MS (ESI+) for C,3H,5C1N202 m/z 267 (M+H)+ Example 66-5-isopropyl-2-[(2,2,6,6-tetramethylpiperidin-4-yl)amino]-l,3-oxazoI-4(5H)-one
[0607] Synthesis was performed from 2-amino-5-isopropyl-l,3-oxazol-4(5H)-one and 4-amino-2,2,6,6-tetramethylpiperidme according to Method G + H. 106081 1H NMR (400 MHz, OMSO-d6) 5 ppm 0.78 - 0.84 (m, 3 H) 0.95 - 1.04 (m, 3 H) 1.33 - 1.43 (m, 12 H) 1.44 - 1.58 (m, 2 H) 1.91 - 2.16 (m, 3 H) 3.96 - 4.09 (m, 1 H) 4.60 (d, J=3.78 Hz, 0.9 H) 4.84 (d, J=4.03 Hz, 0.1 H) 7.83 (d, J=l 1.60 Hz, 0.75 H) 8.16 (s, 0.25 H) 8.76 (d, J=l 1.48 Hz, 1 H) 9.00 (d, J=7.45 Hz, 1 H). MS (ESI+) for C15H27N302 m/z 282 (M+H)+ Example 67-5-isopropyI-2-morpholin-4-yl-l,3-oxazol-4(5H)-one 73
[0609] Synthesis was performed from 2-amino-5-isopropyl-l ,3-oxazol-4(5H)-one and morpholine according to Method G + H. 106101 Ή NM (400 MHz, DMSC ¾ δ ppm 0.81 (d, J=6.84 Hz, 2 Η) 0.87 (d, J=6.84 Hz, 1 H) 0.97 - 1.01 (m, 3 H) 2.02 - 2.17 (m, 1 H) 3.06 - 3.13 (m, 2 H) 3.53 - 3.77 (m, 6 H) 4.66 (d, J=3.91 Hz, 0.67 H) 4.84 (d, J=4.15 Hz, 0.33 H). MS (ESI+) for C,0H16N2O3 m/z 213 (M+H)+ Example 68-5-isopropyI-2-[(2-morpholin-4-ylethyI)amino]-l>3-oxazol-4(5H)-one
[0611] Synthesis was performed from 2-amino-5-isopropyl-l,3-oxazol-4(5H)-one and N-(2-aminoethyl)morpholine according to Method G + H. 106121 !H NMR (400 MHz, DMSO-^) 6 ppm 0.87 (d, J=6.84 Hz, 1 H) 0.92 (d, J=6.84 Hz, 2 H) 1.02 (d, J=6.96 Hz, 3 H) 2.01 - 2.24 (m, 1 H) 2.63 - 2.72 (m, 2 H) 2.72 - 2.81 (m, 1 H) 3.03 (t, J=6.41 Hz, 1 H) 3.08 - 3.36 (m, 3 H) 3.54 - 3.67 (m, 1 H) 3.65 - 3.71 (m, 2 H) 3.75 - 3.86 (m, 2 H) 4.57 (d, J=4.15 Hz, 0.5 H) 4.82 (d, J=4.39 Hz, 0.5 H) 7.32 - 8.39 (m, 1 H). MS (ESI+) for Ci2H2iN303 m/z 256 (M+H)+ Evamn!e 60-2-f4-ben7ivln!neririin-1-vn-5-isnnronvl-1
[0613] Synthesis was performed from 2-amino-5-isopropyl-l,3-oxazol-4(5H)-one and 4-benzylpiperidine according to Method G + H. 106,41 Ή NMR (400 MHz, DMSO-tfd) δ ppm 0.76 - 0.82 (m, 2.25 H) 0.87 (d, J=6.84 Hz, 0.75 H) 0.95 - 1.01 (m, 3 H) 1.07 - 1.35 (m, 2 H) 1.60 - 1.88 (m, 3 H) 2.00 - 2.18 (m, 1 H) 2.53 (d, J=7.08 Hz, 2 H) 2.74 - 2.86 (m, 0.5 H) 2.95 - 3.10 (m, 1.5 H) 3.23 (d, J=12.57 Hz, 0.5 H) 4.03 (d, J=13.55 Hz, 0.75 H) 4.10 (d, J=13.18 Hz, 0.75 H) 4.62 (d, J=3.78 Hz, 0.75 H) 4.84 (d, J=4.15 Hz, 0.25 H) 7.15 - 7.22 (m, 3 H) 7.24 - 7.32 (m, 2 H). MS (ESI+) for Ci8H24N202 m/z 301 (M+H)+ 74 Example 70-2-azocan-l-yI-5-isopropyl-l,3-oxazoI-4(5H)-one
[0616] Synthesis was performed from 2-amino-5-isopropyl- 1 ,3-oxazol-4(5H)-one and heptamethyleneimine according to Method G + H. Ή NMR (400 MHz, DMSO-_¾ δ ppm 0.80 (d, J=6.84 Hz, 3 H) 1.00 (d, J=6.96 Hz, 3 H) 1.32 - 1.43 (m, 1 H) 1.47 - 1.56 (m, 5 H) 1.67 - 1.76 (m, 4 H) 2.04 - 2.13 (; 3.37 - 3.47 (m, 2 H) 3.58 - 3.71 (m, 2 H) 4.64 (d, J=3.54 Hz, 1 H). MS (ESI+) for Ci3H22N202 m/z 239 (M+H)+ Example 71-2-[(cyclohexyImethyl)amino]-5-phenyI-l,3-oxazol-4(5H)-one
[0619] Synthesis was performed from 2-amino-5-phenyl-l,3-oxazol-4(5H)-one and aminomethylcyclohexane according to Method G + H. '^01 lE NMR (400 MHz, DMSO-_ftf) δ ppm 0.92 (m, 2 H) 1.14 (m, 3 H) 1.57 (m, 6 H) 3.14 (m, 2 H) 5.72 (s, 0.7 H) 5.74 (s, 0.3 H) 7.28 (m, 2 H) 7.39 (m, 3 H) 9.00 (t, J=5.74 Hz, 0.7 H) 9.25 (s, 0.3 H). MS (ESI+) for C,6H2oN202 m/z 273 (M+H)+ Example 72-2-(cycIoheptylamino)-5-phenyl-l,3-oxazol-4(5H)-one
[0621] Synthesis was performed from 2-amino-5-phenyl-l,3-oxazol-4(5H)-one and cycloheptylamine accotding to Method G + H. 106221 1H NMR (400 MHz, DMSC ¾ δ ppm 1.35-1.70 (m, 10 H) 1.92 (m, 2 H) 3.78 (m, 1 H) 5.69 (s, 0.75 H) 5.73 (s, 0.25 H) 7.28 (m, 2 H) 7.39 (m, 3 H) 8.92 (s, 1 H). MS (ESI+) for C16H20N2O2 m/z 273 (M+H)+ 75 Example 73-5-benzyl-2-[(cyclohexylmethyI)amino]-l,3-oxazoI-4(5H)-one
[0623] Synthesis was performed from 2-amino-5-benzyl-l ,3-oxazol- (5H)-one and aminomethylcyclohexane according to Method G + H. 106241 Ή NMR (400 MHz, DMSO-t¼) δ ppm 0.7-1.7 (m, 11 H) 2.93 (m, 3 H) 3.16 (m, 1 H) 4.95 (m, 1 H) 7.23 (m, 5 H) 8.56 (s, 1 H). MS (ESI+) for C,7H22N202m/z 287 (M+H)+ Example 74-2-(cycloheptylamino)-5-isopropyl-l,3-oxazol-4(5H)-one
[0625] Synthesis was performed from 2-amino-5-isopropyl-l,3-oxazol-4(5H)-one and cycloheptylamine according to Method G + H. 106261 Ή NMR (400 MHz, DMSO--¾ δ ppm 0.77-082 (m, 3 H) 0.94-1.01 (m, 3 H) 1.32-1.67 (m, 10 H) 1.80-1.90 (m, 2 H) 2.00-2.11 (m, 1 H) 3.62-3.74 (m, 1 H) 4.53 (d, J=3.66 Hz, 0.73 H) 4.57 (d, J=3.66 Hz, 0.27 H) 8.80 (d, J=8.06 Hz, 0.73 H) 9.06 (s, 0.23 H). MS Example 75-2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-l,3-oxazol-4(5H)-one
[0627] Synthesis was performed from 2-amino-5-isopropyl-l,3-oxazol-4(5H)-one and bicyclo[2.2.1]hept-2-amine according to Method G + H. 106281 1H NMR (400 MHz, OMSO-d6) δ ppm 0.75-0.84 (m, 3 H) 0.93-1.02 (m, 3 H) 1.03-1.17 (m, 3 H) 1.34-1.52 (m, 4 H) 1.60-1.71 (m, 1 H) 1.98-2.25 (m, 3 H) 3.46-3.53 (m, 1 H) 4.50-4.58 (m, 1 H) 8.67 (s, 1 H). MS (ESI+) for Ci3H20N2O2 m/z 237 (M+H)+ 76 Example 76-2-(bicyclo[2.2.1]hept-2-yIamino)-5-isobutyI-l,3-oxazol-4(5H)-one
[0630] Synthesis was performed from 2-amino-5- isobutyl-l,3-oxazol-4(5H)-one and bicyclo[2.2.1 ]hept-2-amine according to Method G + H. 106311 Ή NM (400 MHz, CHLOROFORM-D) δ ppm 0.93 - 1.02 (m, 6 H) 1.08 -1.37 (m, 3 H) 1.42 - 1.97 (m, 8 H) 2.28 - 2.41 (m, 2 H) 3.55 - 3.62 (m, 0,8 H) 3.75 - 3.83 (m, 0.2 H) 4.57 - 4.63 (m, 0.2 H) 4.68 - 4.75 (m, 0.8 H) 10.21 (s, 1 H)
[0632] MS (ESI+) for C14H,7N303 m/z 251 (M+H)+ Example 77-2-(cycloheptylamino)-5-isobutyl-l,3-oxazol-4(5H)-one
[0633] Synthesis was performed from 2-amino-5- isobutyl-l,3-oxazol-4(5H)-one and cycloheptylamine according to Method G + H. 106341 !H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.93 - 1.01 (m, 6 H) 1.37 -2.10 (m, 15 H) 3.71 - 3.82 (m, 0.65 H) 3.92 - 4.02 (m, 0.35 H) 4.60 (dd, J=10.07, 2.99 Hz, 0.35 H) 4.66 (dd, J=9.89, 3.05 Hz, 0.65 H) 9.38 (s, 1 H)
[0635] MS (ESI+) for C14H17N303 m/z 253 (M+H)+ Example 78-5-isobutyI-2-[(2-methylphenyl)amino]-l,3-oxazol-4(5H)-one
[0636] Synthesis Was performed from 2-amino-5-isopropyl-l ,3-oxazol-4(5H)-one and 2-methylphenylamine according to Method G + H: 106371 1H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.93 - 1.03 (m, 6 H) 1.64 -1.76 (m, 1 H) 1.81 - 1.95 (m, 2 H) 2.35 (s, 3 H) 4.82 - 4.89 (m, 1 H) 7.22 - 7.31 (m, 4 H)
[0638] MS (ESI+) for Ci4HnN303 m/z 247 (M+H)+ 77 Example 79-2-(bicyclo [2.2.1 ] hept-2-yIamino)-5-isopropyl-5-methyl-l , 3-th iazol-4(5H> one
[0639] To a solution of 2-amino-2,3-dimethylbutanoic acid (400 mg, 3.05 mmol) and potassium bromide (1.190 g, 10.00 mmol) in H20 (4 mL) and concentrated H2S04 (345 μΐ ) at 0 °C under stirring was added via a syringe over 50 min a solution of NaN0 (295 mg, 4.27 mmol) in H20 (900 μΐ,). The reaction was allowed to slowly reach ambient temperature, and was then stirred overnight. The resulting solution was extracted with diethyl ether (2 x 15 mL), and the combined organic phases were washed with brined and dried over MgS04. The solvent was removed to give a transparent oil (290 mg), Which was used without any further purification. A mixture of the crude oil (250 mg) and N-bicyclo[2.2. l]hept-2-ylthiourea (F18616001) (100 mg, 0.587 mmol) in 1,4-dioxane (600 was stirred at 100 °C in a sealed tube for 3 days. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC chromatography to give the product as a white solid. l0640] Ή MR (400 MHz, CDC13) δ 0.85-0.88 (m, 3 H), 0.99-1.04 (m, 3 H), 1.10-1.27 (m, 4 H), 1.46-1.58 (m, 2 H), 1.61-1.65 (m, 3 H), 1.71-1.88 (m, 2 H), 2.12-2.23 (m, 1 H), 2.27-2.42 (m, 2 H), 3.35 (m, 0.8 H, major isomer), 4.03 (m, 0.2 H, minor isomer).
MS (ESI+) for C,4H22N2OS m/z 267 (M+H)+.
GENERAL METHODOLOGIES K-PP Methodologies for Synthesis of Starting Materials: Carboxylic Acids, Esters, Acid Chlorides, Acyl Isothiocyanates: METHOD K
[0641] The thioisocyante intermediates can be prepared by the method K.
Formation of the acid chloride, such as by treatment with oxalyl chloride and DMF, or thionyl chloride, followed by treatment with KNCS provides the thioisocyantes.
Alternatively, treatment of the carboxylic acid with thionyl chloride, then bromination, such as with Br2 and PBr3} followed by treatment with KNCS also provides the thioisocyantes. 78 METHOD L
[0642] Preparation of bromo substituted esters and carboxylic acids is described in Method L. Bromination of the carboxylic acid, such as with Br2) PC13 (cat.), followed by formation of the acid chloride, such as by treatment with oxalyl chloride or thionyl chloride, and treatment with alcohols, TMSCHN2 or CH2N2, yields the desired compounds.
Alternatively, the acid chloride can be formed first, followed by bromination step. Starting from esters, treatment with strong base, e.g. LDA, and a leaving group supplier such as TMSC1, followed by bromination provides the desired esters. Using amino acid starting materials (A= H2) , bromination, such as by reaction with HBr in the presence of NaN02, yields the desired bromo acids.
METHOD M D, E, J = CH or N
[0643] Methylation of various substituted acids and esters, such as by treatment with base and an methyl halide, followed by bromination, yields the desired a-bromo- -methyl compounds.
METHOD N
[0644] Conversion of various ketones to the esters is accomplished by Method N. Treatment with an appropriate dithiane, such as 2-trimethylsilyl-l,3-dithiane, in the presence of base, e.g. n-BuLi, followed by chlormatiori, such as with N-chlorosuccinimide, yields the desired compounds. 79 Methodologies for Synthesis of Starting Materials: Thioureas and Amines: METHOD O
[0645] Formation of the desired thioureas is detailed in Method O. Treatment of amines with BzNCS, followed by deprotection, such as with base, yields the thioureas.
Alternatively, the thiourea is formed through treatment with 1,1-thiocarbonyldiimidazole in the presence of base, e.g. NEt3, followed by treatment with ammonia.
METHOD P
[0646] Alternatively, the thiourea is formed as described in Method P. Treatment of a substituted thioisocyanate with ammonia yields the desired thioureas.
METHOD Q IU047] Preparation ot substituted bicyclo|_2.2.1Jheptane amines is described synthetic scheme in shown in Example 97.
METHOD R
[0648] Preparation of 1 -amino- 1-methylethyl benzenes is described in Method R. Methylation of cyanomefhylbenzenes, such as with treatment with methyl halides in the presence of non-nucleophilic base, e.g. KHMDS, yields the 1-cyano-l-methylethyl benzenes. Oxidation of the cyano compounds, such as with H202, in the presence of base, e.g. K2CO3, yields the amides. Hofmann rearrangement of the amides, such as by treatment with (O2CCF3)2-Ph, yields the desired amines. 80 METHOD S
[0649] Bicyclo[2.2.1]heptanyl thioureas are provided via Method S. Bromination of carboxylic acids, such as with Br2, PC13, and the resulting rearrangement provides the 2-bromo-1 -carboxylic acids. Dehalogenation, such as with Zn in AcOH, yields the 1-carboxylic acids. The Curtius rearrangement such as by treatment with DPPA and a base, e.g. Et3, and an alcohol provides the protected amine. Deprotection, such as with acid, followed by formation of the thiourea and deprotection, as described above, provides the desired thioureas.
METHOD T
[0650] Base mediated substitution of a nitrophenol with a alkyl halide, provides the nitophenyl ether. For example Cs2C03 can be used in the presence of Nal. Reduction of the nitro group, such as with ¾ in the presence of a catalyst, e.g. Pd/C, yields the desired amines.
METHOD U
[0651] Method U describes the formation of cyclopropanamines from benzonitriles is accomplished by treatment with EtMgBr in the presence of Ti(Oz'-Pr)4, followed by treatment with BF3eOEt2.
METHOD V
[0652] Formation of bicyclo[2.2.2]octanyl amines is described in Method V. De-esterification of the esters, such as with base, e.g. LiOH, followed the Curtius rearrangement as described previously and deprotection, e.g. acid, provides the desired amines.
METHOD W
[0653] Formation of (bicyclo[2.2. l]heptanylmethyl)-thioureas from the carboxylic acids is described in Method W. Formation of the acid chloride, such as by treatment with oxalyl chloride and DMF (cat.), followed by treatment with ammonia or ammonium hydroxide, provides the amide. Reduction of the amide, such as with treatment with LiAfflU, to the amine, followed by chemistry previously described, yields the desired thioureas.
Methodologies for Synthesis of Final Products: METHOD X Method X. Treatment of a bromo-substituted carboxylic acid or ester with thiourea in the presence of base, such as DIEA provides the condensation/ring closure to the desired 2-amino-thiazolones.
METHOD Y
[0655] Alternatively, as shown in Method Y, treatment of a bromo-substituted carboxylic acid with thiourea in the presence of base, such as NaOAc provides the condensation/ring closure to the desired 2-amino-thiazolones. 82 METHOD Z
[0656] Thiazolones also can be prepared from amines by the method described in Method Z. Coupling of an amine with an isothiocyante, e.g. in the presence of base, such as NEt3, provides the condensation/ring closure to the desired 2-amino-thiazolones.
METHOD AA [0657J 5,5-Disubstituted thiazolones can be prepared from thiazolones via the method described in Method AA. Treatment first with strong base, e.g. LDA or NaHMDS, then with a compound comprising an appropriate leaving group, such as RB-LG, provides the desired compounds.
METHOD BB
[0658] Similarly, formation of 5-fluoro-thiazolones can be prepared as described, in Method BB. Treatment first with strong base, e.g. LDA or NaHMDS, and TMSCl, followed by fluorination, e.g. with Selectfluor, provides the desired compounds.
METHOD CC
[0659] Similarly, formation of 5-trifluoromethyl-thiazolones ban be prepared as described in Method CC. Treatment first with strong base, e.g. LDA or NaHMDS, and 83 TMSCl, followed by tnfluoromethylation, e.g. with -?-(trifluoromethyl)dibenzothioph salt, provides the desired compounds.
METHOD DD
[0660] Formation of 5-carboxymethyl-thiazolones or the corresponding esters can be prepared as described in Method DD. Coupling of carboxylic acids with a substituted alkene, such as in the presence of DBU, followed by treatment with base, e.g. Li OH, provides the desired compounds.
METHOD EE
[0661] Formation of 5-spiro-thiazolones can be prepared as described in Method EE. Coupling of the thiazolone in the presence of strong base, e.g. LDA or NaHMDS, alkylation first with base, e.g. HMDS, dn the presence of TMSCl; followed by further treatment with base, e.g. LDA, in the presence of a bis-electrophile.
METHOD FF
[0662] Formation of 5-hydroxymethyl-thiazolones can be prepared as described in Method FF. Treatment of a thiazolone with a ketone in the presence of strong base, e.g. LDA or NaHMDS, provides the desired compounds. 84 METHOD GG
[0663] Formation of 5-fluoromethyl-thiazolones can be prepared as described in Method GG. Fluorination of 5-hydroxymethyl-thiazolones e.g. with DAST or Deoxo-Fluor, provides the desired compounds.
METHOD HH
[0664] The compounds of the invention can be prepared by the method described in this scheme. Alkylation of the racemic thiazalone with a chiral base, such as where Rm and Rn are independently selected from alkyl, aryl, and heterocyclyl, where R° and Rp are independently selected from aryl, where J is alkyl, O, ΝΉ or S, and where M1 and M2 are independently selected from Li, Na, K, Cs, Cu, Zn, and Mg, e.g. a chiral lithium base, more specifically and an appropriate alkylating agent, such as a alkyl halide (e.g. an alkyl iodide) or sulfonate (e.g., mesylate, triflate), [LG is halide, tosylate, mesylate, triflate, or the like] provides the desired chiral di^substituted thiazolone.
Preferably, the alkylation is performed in the presence of amine base, such as TMEDA.
Treatment with the R,R form of the base provides the stereochemistry shown when R3 is methyl. Treatment with the S,S form provides the opposite stereochemistry to that shown when R3 is methyl. The reaction is maintained at a temperature below about RT, preferably below about 0 °C, more preferably at or below about -15 °C. An aprotic solvent, e.g. toluene is acceptable. 85 METHOD II
[0665] Formation of thiazolone amines and ethers can be prepared as described in Method II. Bromination of thiazolones e.g. with NBS or other techniques known to one skilled in the art, followed by treatment with an amine or alcohol, provides the desired compounds.
METHOD JJ
[0666] Formation of thiazolone amines can be prepared from the alcohols as described in Method JJ. Following the procedure for the Dess-Martin Periodinane or Swem reactions, followed reductive amidation, such as with reacting with an amine together with NaBH(OAc)3 or NaB¾CN, provides the desired compounds.
METHOD KK
[0667] Alternatively, formation of 5-spiro-thiazolones can be prepared from the furanone as described in Method KK. Treatment of the furanone with a thiourea provides thiazolone alcohol. Protection of the alcohol, such as with dihydropyran in the presence of acid, followed by treatment with strong base, e.g. LDA, and 3-bromo-2-methylprop-l-ene, and deprotection , e.g. with PTSA, and cyclization, such as with acid, provides the desired compounds. 86 METHOD LL
[0668] Further, formation of 5-spiro-thiazolones can be prepared from the thiazolone as described in Method LL. Treatment of the thiazolone with strong base, e.g. LDA or NaHMDS and alkylation, such as with (2-bromoethoxy)(tert-butyl)dimethylsilane provides the protected thiazolone alcohol. A subsequent round of base and silane provides the disubstituted thiazolone. Deprotection , e.g. with acid, followed with addition of a compound containing an appropriate leaving group, e.g. MsCl, in the presence of base, e.g. DIEA, and cyclization, such as with a substituted amine, provides the desired spiro piperidine compounds.
METHOD MM
[0669] 1-Substituted piperidinefnethylthiazolones can be prepared by method MM. After deprotection, such as by treatment with acid, treatment with sulfonyl chlorides (R12S02C1) in the presence of base, e.g. NEt3, provides compounds where RQ = S02Rs. Alternatively, after deprotection, treatment with carboxylic acid (RRC02H) with standard coupling chemistry, e.g. EDCI, and HOBt, provides compounds where RQ = CORR.
Alternatively, after deprotection, treatment with active carbonyl compounds, e.g. acid anhydrides (RRCO-0-CORR) in the presence of base, e.g. DIEA, provides compounds where RQ = CORR.
METHOD NN 87
[0670] Formation of 5-spiro-thiazolones can be prepared from the thiazolone as described in Method NN. Treatment of the thiazolone with strong base, e.g. LDA and alkylation, such as with BrCH2CH2Br provides the thiazolone bromoethyl compound.
Further treatment with strong base, e.g. LDA, and dimethylketone, provides the desired spiro tetrahydrofuryl compounds.
METHOD OO
[0671] Substituted amidomethylthiazolones can be prepared by method OO.
Treatment of a substituted thioureas and with active carbonyl compounds, e.g. maleic anhydride in the presence of acid, e.g. AcOH, provides the thiazolone carboxylic acids. Treatment of the acid with an amine, such as in the presence of a coupling reagent, e.g. HATU and base such as DJJSA provides the desired amides.
METHOD PP D, E, J = N or CH
[0672] Substituted thiazolone esters can be prepared from the alcohol by method PP. Treatment of an alcohol-substituted thiourea with active carbonyl compounds, e.g. an acid chloride, in the presence of base, e.g. DIEA, provides the desired esters. Separation Methods
[0673] Many of the final compounds were separated by two main chromatographic methods. Normal phase liquid chromatography (NPLC) and supercritical fluid chromatography (SFC) were the two techniques utilized. NPLC was performed with Chiralpak AD/AD-H and Chiralcel OJ-H columns. The mobile phase consisted of hexane (0.2% diethylamine (DEA)) and/or methanol, ethanol (0.2% DEA), or isopropanol (0.2% DEA). All separations were conducted at ambient temperatures. Columns used with SFC 88 were the Chiralpak AD-H and AS-H, the Chiralcel OD-H, and the Astec (R,R) P-CAP. The mobile phased was comprised of liquid carbon dioxide and an organic modifier such as methanol (with or without 0.2% DEA), ethanol (with or without 0.2% DEA), isopropanol (with or without 0.2% DEA), or acetonitrile (with or without 0.2% DEA). Organic modifiers were used individually with liquid carbon dioxide or in combinations with each other and the liquid carbon dioxide. Column/oven temperature was between 35 and 40 °C, and the outlet pressure was either 100 or 120 bar.
Illustrative method for separating enantiomers of thioureas:
[0674] Stationary phase: ChiralPA -AD, 20u, from Chiral Technology
[0675] Column: MODCOL spring load column, 4"x30cm containing of 2.0 kg of stationary phase.
[0676] Mobile phase: 100% MeOH
[0677] Flow rate: 500ml/min
[0678] Temperature: 30 °C .
[0679] Detection wavelength: 230 nm Abbreviations
[0680] ΑΓΒΝ, 2,2'-Azobisisobutyronitrile
[0681] aq., aqueous
[0682] brine, a saturated solution of NaCl in water
[0683] cone, concentrated
[0684] DAST, Diethylaminosulfur trifluoride
[0685] DBU, l,8-Diazabicyclo[5.4.0]undec-7-ene
[0686] DCM, dichloromethane
[0687] DEAD, diethyl azodicarboxylate
[0688] Deoxo-Fluor, Bis(2-methoxyethyl)aminosulfur trifluoride
[0689] Dess-Martin Periodinane, l,l,l-Tris(acetyloxy)-l,l-dihydro-l,2-benziodoxol-3(lH)-one
[0690] DTEA, N,N-Diisbpropylethylamine
[0691] DMF, N,N-Dimethylformamide
[0692] DPP A, Diphenylphosphoryl azide
[0693] EDCI, l-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride 89
[0694] EtOAc, ethyl acetate
[0695] EtOH, ethanol
[0696] HOBT, 1-Hydroxy-lH-benzotriazole
[0697] Hunig's base, N,N-Diisopropylethylamine
[0698] KHMDS, Potassium bis(trimethylsilyl) amine
[0699] LDA, Lithium diisopropylamide
[0700] LiHMDS, Lithium bis(trimethylsilyl)amine
[0701] MeOH, methanol
[0702] (Λ)-ΜΟΡ, (R)-(+)-2-(diphenylphosphino)-2'-methoxy- 1 , 1 '-binaphthyl
[0703] MS; Mass Spectrum
[0704] MsCl, Methanesulfonyl chloride
[0705] MTBE, methyl ierf-butyl ether
[0706] MW, microwave
[0707] NaHMDS, Sodium bis(trimethylsilyl)amine
[0708] BS, N-Bromosuccinimide
[0709] n-BuLi, n-Butyllithium
[0710] PCC, Pyridinium chlorochromate
[0711] i-PrOH, wo-propanol
[0712] PTSA, p-toluenesulfonic acid
[0714] sat'd, saturated solution in water
[0715] Selectfluor™, N-Fluoro-A^-chloromethyltriethylenediamine bis(tetrafluoroborate)
[0716] TBDMS, tert-butyl dimethylsilyl
[0717] THF, Tetrahydrofuran
[0718] TLC, thin layer chromatography
[0719] TMSC1, chlorotrimethylsilane Synthesis of Starting Materials: Carboxylic Acids, Esters, Acid Chlorides, and Acyl Isothiocyanates (procedures METHOD-L, METHOD-M, METHOD-N, METHOD-K).
[0720] Unless otherwise noted, all materials were obtained from commercial suppliers and used without further purification. All parts are by weight and temperatures are 90 in degrees centigrade unless otherwise indicated. All microwave-assisted reactions were conducted with a Smith Synthesizer from Personal Chemistry, Uppsala, Sweden or a Discover Instrument from CEM, Matthews, North Carolina. All compounds showed NMR spectra consistent with their assigned structures. Melting points were determined on a Buchi apparatus and are uncorrected. Mass spectral data was determined by electrospray ionization technique. All examples were purified to >95% purity as determined by high-performance liquid chromatography. Unless otherwise stated, reactions were run at RT.
Example 80-(iS)-2-Bromo-3-rnethylbutanoic acid.
Br-^C02H METHOD L
[0721] A 2 L j acketed reactor was charged with toluene (150 mL), water (150 mL) and 48% hydrobromic acid (260 mL, 2.30 mol). To this stirred, two-phase solution at 0 °C, was added L-valine (96.2 g, 0.82 mol) in one portion (a mild exotherm was observed, temperature rose to 3.5 °C). The mixture was further cooled to -5 °C, whereupon an aqueous solution of sodium nitrite (73.7 g, 1.07 mol) was added drop-wise over 6 h. The solution turned dark brown. Once the sodium nitrite was completely added, the reaction mixture was stirred for an additional 3 h at -5 °C. Then, the reaction mixture was diluted with toluene (250 mL), warmed to 20 °C, and stirred for 12 h. The organic layer was separated and the aqueous layer was extracted with toluene (300 mL). The toluene layers were combined and washed with a 20% sodium thiosulfate solution (200 mL) (virtually all color disappeared) followed by a 20% NaCl solution (200 mL). The organic layer was separated, and the solvent was concentrated in vacuo, and then placed on the high vacuum pump for 4 h to afford the title compound (107 g) as a pale yellow crystalline solid. MS (ESI, pos. ion) m/z: 179.1/180.9.
Example 81-1-Bromocyclopentanecarboxylic acid.
METHOD L 91
[0722] Phosphorus trichloride (0.54 mL, 6.20 mmol) was added drop-wise to the mixture of cyclopentanecarboxylic acid (14.2 g, 124 mmol) and bromine (7.35 mL, 143 mmol). The mixture was then gradually heated to 85 °C and stirred at this temperature in a sealed vessel for 12 h. After cooling to ambient temperature, the mixture was partitioned between EtOAc and water. The organic portion was separated, washed with water and brine, and cone, in vacuo to give the title compound as a white solid.
Example 82-Ethyl 1-bromocyclopentanecarboxylate.
[0723] DMF (a few drops) was added to a mixture of 1-bromocyclopentane-carboxylic acid (23.9 g, 124 mmol) and oxalyl chloride (11.6 mL, 130 mmol) in 250 mL of CH2CI2. The mixture was stirred at ambient temperature for 2 h. After removing the low-boiling solvents in vacuo, ethanol (50 mL) was added to the residue followed by the addition of N,N-diisopropylethylamine (22.7 mL, 130 mmol). The mixture was stirred at ambient temperature for 20 min. After removing the low-boiling solvents in vacuo, the residue was partitioned between diethyl ether and water. The organic portion was washed with water and brine, and cone, in vacuo. The crude product was filtered through a plug of silica gel using 0 Example 83-Methyl 2-bromo-2-cyclohexyIacetate.
METHOD L
[0724] A 100 mL round-bottomed flask was charged with cyclohexylacetic acid (5.0 g, 0.035 mol) and thionyl chloride (4.92 g, 3.0 mL, 0.041 mol). This solution was heated to reflux during which time gas evolution occurred. After lh at 80 °C, bromine (7.03 g, 2.25 mL, 0.044 mol) and phosphorus tribromide (0.350 mL) were added. The reaction temperature was maintained at 80 °C until the color faded from dark red to a light pink (~2 h) 92 after which time MeOH (5.0 mL) was added, and the reaction mixture was refluxed for 30 min more. After cooling to room temperature, sodium thiosulfate was added, the suspension was filtered, and then concentrated in vacuo to provide the title compound. This bromo-ester was used without any further purification.
Example 84-Methyl 2-bromo-2-(tetrahydro-2/-r-pyran-4-yI)acetate.
METHOD L
[0725] A 250 mL round-bottomed flask was charged with 2-(tetrahydro-2H-pyran-4-yl) acetic acid (5.0 g, 0.035 mol) and 100 mL of MeOH. To this solution was added 5 drops of cone. ¾S04. This mixture was heated at reflux for 12 h, after which time the MeOH was removed in vacuo. The remaining residue was dissolved in EtOAc, washed with saturated aqueous NaHC03) dried, and concentrated in vacuo to give the desired methyl ester. This compound was used directly in the next step without further purification.
[0726] To a dry 250 mL round-bottomed flask was added 2.20 g of methyl 2-(tetrahydro-2H-pyran-4-yl)acetate (0.014 mol) and 100 mL of dry THF. This solution was cooled to -78 °C and LDA (2.0 M in THF/heptane/ethyl benzene, 10.4 mL, 0.021 mol) was added. The resulting brown solution was stirred at -78 °C for 45 min. TMSC1 (3.22 g, 3.5 mL, 0.028 mol) was then added at -78 °C, and the reaction mixture was then warmed to room temperature. After being re-cooled to -78 °C, N-bromosuccinimide (4.94 g, 0.028 mol) was added to the reaction mixture, and the resulting suspension was allowed to slowly warm to room temperature where it continued to stir for an additional 1.5 h. The suspension was then filtered thru a pad of Si02 using diethyl ether as the eluant. Purification of the filtrate by column chromatography (Si02 gel, 10: 1 to 4:1 hexanes/ethyl acetate) delivered the desired a-bromo ester, which was used in subsequent steps without further purification. 93 Example 85-Ethyl 2-(pyridin-4-yl)propanqate.
METHOD M
[0727] To a solution of LiN(TMS)2 (Aldrich, 1.0 M solution in THF, 30 mL, 30 rnmol) in THF (30 mL) was added ethyl 4-pyridylacetate (Aldrich, 4.7 mL, 30 mmol) ) at 0 °C. Methyl iodide (Aldrich, 2.4 mL, 38 mmol) was added 30 min later. After 1 h, the reaction mixture was concentrated in vacuo. The crude product was purified by silica gel chromatography. Mass Spec, m/z + ion 180 (M+l).
Example 86-Ethyl 2-bromo-2-(pyridin-4-yl)propanoate
[0728] The above compounds were prepared according to the procedure reported in-the literature: see D. Yang, J Org. Chem. 2002, 67, 7429.. MS: 258, 260 (M+l). To a solution of ethyl 2-(pyridin-4-yl)propanoate (5.3 g, 30 mmol), Mg(C104)2 (Aldrich, 2.0 g, 9.0 mmol) in C¾CN (60 mL) was added N-bromosuccinimide (Aldrich, 5.9 g, 33 mmol) at Na2C03. The organic phase was separated, dried over Na2S04, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography. Mass Spec, m/z + ion 258, 260 (M+l).
Example 87-Ethy] 2-bromo-2-(pyridin-3-yI)propanoate.
[0729] To a stirred mixture of ethyl 2-(pyridin-3-yl)propanoate (4.2 g, 23 mmol), CCI4 (100 mL), and N-bromosuccinimide (Aldrich, 4.6 g, 26 mmol) was added 2,2'-azobisisobutyronitrile (Aldrich, 0.8 g, 5 mmol) under N2 at room temperature. The mixture 94 was gradually heated to reflux. After 7 h, the reaction mixture was concentrated in vacuo. The crude was purified by silica gel chromatography. Mass Spec, m/z + ion 258, 260 (M+l ).
Example 88-4-(l,3-Dithian-2-yIidene)-6-fluoro-3,4-dihydro-2H-chromene.
METHOD N
[0730] To a solution of 2-trimethylsilyl-l,3-dithiane (5.10 g, 26.5 mmol) in 50 mL of anhydrous THF at -60 °C under N2 was added drop-wise «-BuLi (1.6 M solution in hexanes, 16.6 mL, 26.5 mmol). The mixture was left to warm slowly to 0 °C over 3 h and subsequently cooled to -60 °C. A solution of 6-fluoro-2,3-dihydrochromen-4-one (4.40 g, 26.5 mmol) in 25 mL of THF was added drop-wise. The mixture was slowly warmed to ambient temperature overnight, then poured into water, and extracted with EtOAc. The combined organic portions were washed with brine, and cone, in vacuo. The crude product was purified by flash column chromatography (0 to 10% of EtOAc in hexanes). The title compound was obtained as a pale oil.
Example 89-Ethyl 4-chloro-6-fluoro-3,4-dihydro-2H-chromene-4-carboxylate.
[0732] A solution of 4-(l,3-dithian-2-ylidene)-6-fluoro-3,4-dihydro-2H-chromene (4.60 g, 17.1 mmol) in 45 mL of anhydrous THF in an addition funnel was added drop-wise to a stirring solution of N-chlorosuccinimide (11.7 g, 85.7 mmol) in 100 mL of C¾CN arid 50 mL of EtOH at r.t. After 3 h, 50 mL of water was added. The mixture was partitioned between EtOAc and water. The combined organic portions were washed with brine, and cone, in vacuo. The residue was purified by flash column chromatography (0 to 10% of EtOAc in hexanes). The title compound was obtained as a colorless oil. 95 Example 90-( ?)-2-Bromo-3-methylbutanoyI chloride.
METHOD K (0733] To a 500mL round-bottom flask was added 5.0 g (27.6 mmol) of (R)-2-bromo-3-methylbutanoic acid and 200 mL CH2CI2. The resulting solution was cooled to 0°C in an ice bath and then 3 mL of oxalyl chloride (34.4 mmol) was added in one portion. After 5 min, 0.2 mL of DMF (2.59 mmol) was added drop-wise. Once the addition was completed, the mixture was warmed to room temperature and stirred for 4 h. The mixture was then concentrated, triturated with hexanes (50 mL), and filtered. The residual solid was washed with hexane (2 x 10 mL) and the combined supernatant liquids were concentrated to afford the title compound as a pale yellow oil.
Example 91-(-R)-2-Bromo-3-methylbutanoyl isothiocyanate.
[0734] A 100 mL round-bottom flask was charged with KNCS (0.786 g, 8.08 solid was completely dissolved. A solution of (J?)-2-bromo-3-methylbutanoyl chloride (1.51g, 7.55 mmol, 1.0 equiv) in acetone (2 mL) was added drop-wise resulting in the formation of a white precipitate with concomitant color change of the solution from clear to pink to reddish orange. Once addition was complete, the mixture was stirred for 30 min at room temperature. The reaction mixture was then filtered through Celite in a sintered glass (medium porosity) funnel, and washed twice with acetone (10 mL each wash). The deep red solution was concentrated, taken up in hexanes (40 mL), and re-filtered. Concentration afforded the title compound as an orange oil. 96 Synthesis of Starting Materials: Thioureas and Amines (procedures: METHOD-O, METHOD-P, METHOD-Q, METHOD-R, METHOD-S, METHOD-T, METHOD-U, METHOD-V, METHOD- ).
Example 92 (±)-e 0-l-(Bicyclo[2.2.1]heptan-2-yl)thiourea.
METHOD O
[0735] To a stirred solution of 1,1-thiocarbonyldiimidazole (1.94 g, 10.9 mmol) and triethylamine (3.0 mL, 21.8 mmol) in dichloromethane (22.0 mL) under nitrogen was added (±)-endo-2-aminonorborane HCl (1.21 g, 10.9 mmol) over 10 min at ambient temperature for 3 h. The solvent was then evaporated in vacuo, and the residue was dissolved in a 0.5M solution of-arnmonia in dioxane. After stirring at room temperature under nitrogen- for 16 h, the resulting solid was filtered off, and the filtrate was evaporated in vacuo. Upon scratching the glass, the residue crystallized. The solid was placed on the high vacuum pump overnight to afford the title compound (1.16 g) as a brown crystalline solid. MS (ESI, pos. ion) m/z: 171.2 (M+H).
Example 93-l-Benzoyl-3-cyclooctylthiourea.
METHOD O
[0736] Benzoyl isothiocyanate (7.40 mL, 54.0 mmol) was added to a solution of cyclooctananiine (6.25 g, 49.1 mmol) in 200 mL of chloroform. The mixture was stirred at ambient temperature overnight. The solvents were removed in vacuo to give the title compound as a viscous light yellowish oil. MS m/z: 291.0 (M+H)+. 97 W 2005 116002 Example 94-1-Cycloocrylthiourea.
[0737] A mixture of 1 -benzoyl-3-cyclooctylthiourea ( 14.3 g, 49.1 mmol) and potassium carbonate (34.6 g, 250 mmol) in methanol (200 mL), water (100 mL), and THF (100 mL) was stirred at ambient temperature overnight. The low boiling solvents were removed in vacuo, and the residue was partitioned between EtOAc and water. The organic portion was washed with brine, and concentrated in vacuo. The title compound was obtained as a white solid after flash column chromatography (0 to 100% of ethyl acetate in hexanes). MS m/z: 187.1 (M+H)+.
Example 95-(±)-e.vi>-l-(Bicyclo[2.2.1]heptan-2-yl)thiourea.
METHOD P
[0738] A solution of exo-2-norbornylisothiocyanate (32.2 mL, 326 mmol) in 0.5M solution of ammonia in dioxane (1.3 L, 652 mmol) in a 2 L round-bottomed flask was stirred further dried under high vacuum to afford the title compound (39.0 g) as a white amorphous solid. MS (ESI, pos. ion) m/z: 171.2 (M+H).
Example 96-1-Adamantylthiourea.
METHOD-P
[0739] A mixture of 1-adamantyl isothiocyanate (4.83 g, 25.0 mmol, Aldrich) and ammonia (0.5 M solution in 1,4-dioxane, 100 mL, 50 mmol) was stirred at ambient temperature for 48 h. The solvents were removed in vacuo to give the title compound as a white solid. MS m/z: 211.1 (M+H)+. 98 Example 97
[0740] [0741]
[0742] (i)HSiCl3, allyl palladium(II) chloride, ( )-MOP, -3 °C, 3 days; (ii)MeOH, Et3N, Et20, 0 °C to r.t., overnight; (iii)KHF2, urea-H202, Mn02, MeOH, 60 °C, overnight; (iv) PhCH2Br, NaOH, 15-Crown-5, THF, 10 °C, 3h; (v)PCC, CH2C12, 0 °C - r.t., overnight; (vi)Deoxo-Fluor, BF3 - Et2O (0.1 eq), 55 °C, 33 h; (vii)H2, Pd/C, MeOH, r.t.,3 h; (viii)L-Selectride, THF, -78 °C, 3h; ¾O2, NaOH, 65 °C,10 h; (ix)Phthalimide, Ph3P, DEAD, THF, r.t., 70 h; (x)H2NNH2, EtOH, reflux, 5h; HCl(aq), 60 °C, 1.5 h; (xi) PhC(O)NCS, Et3N, CHC13, r.t.; (xii)K2CO3, MeOH/THF/H2O, r.t. 99 (lR,2S,4R,5S)-2,5-Bis(trichIorosilyl) -bicyclo[2.2.1]heptane METHOD Q
[0743] A solution of allylpalladium(II) chloride (0.0180 g, 0.0492 mmol) and (R)-(+)-2-(diphenylphosphino)-2'-methoxy-l,l'-binaphthyl (0.105 g, 0.223 mmol) in benzene (2.5 mL) was placed into a double-jacketed 250-mL three-neck flask equipped with a mechanical stirrer under nitrogen atmosphere. Trichlorosilane (20.0 mL, 198 mmol) was added, and the mixture was cooled to -3 °C. Bicyclo[2.2.1]hepta-2,5-diene (8.3 mL, 76.9 mmol) was added slowly with mechanical stirring. After stirring at -3 °C for 69 h, the color of the mixture turned into a pale yellowish solid. The reaction mixture was dissolved in toluene (anhydrous, 60 mL), and then concentrated in vacuo to give a pale solid, which was used in the following reaction without further purification.
Example 98- (lR,2S,4R,5S)-2,5-Bis(trimethoxysilyl)bicyclo[2.2.1]heptane.
[0744] A mixture of methanol (anhydrous, 60 mL), triethylamine ( anhvdrous, 80 mL), and diethyl ether (anhydrous, 50 mL) was added slowly to (lR,2S,4R,5S)-2,5-bis(trichlorosilyl) -bicyclo[2.2.1]heptane (crude from the previous reaction, 76.9 mmol) in diethyl ether (anhydrous, 50 mL) at 0 °C under a nitrogen atmosphere. After the mixture was stirred at ambient temperature overnight, the precipitated salts were removed by filtration. The solids were washed with diethyl ether (50 mL x 3). The combined filtrates were concentrated in vacuo to yield a light yellow slurry which was used in the next reaction without further purification.
Example 99-(lR,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diol. 100
[0745] To (lR,2S,4 )5S)-2,5-bis(trimethoxysilyl)bicyclo[2.2.1]heptane (76.9 mmol) was added potassium hydrogen fluoride (33.0 g, 423 mmol), tetrahydrofuran (80.0 mL), methanol (80.0 mL), and urea hydrogen peroxide addition compound (65.0 g, 691 mmol, Aldrich). The resulting white slurry was stirred overnight at 60 °C. After cooling to ambient temperature, Mn02 (0.56 g, 6.4 mmol) was added, and the mixture was stirred at this temperature for 4 h. The solids were removed by filtration, and the filter cake was washed with methanol. The combined filtrates were concentrated in vacuo. The residue was dissolved in water (100 mL) and extracted with a CHCl3/z'-PrOH mixture (3/1, v/v, 5 x 100 mL). The combined organic portions were dried over MgS0 and cone, in vacuo. After triturating the residue with CH2C12 and EtOAc, the white solid was collected by filtration. This material was the title compound. A second crop of desired product was obtained by flash column chromatography (0-5% MeOH in EtOAc) from the concentrated filtrate.
Example 100-(lR,2S,4R,5S)-S-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol.
[0746] To a stirred solution of (lR,2S,4R,5S)-bicycio[2.2.1]-heptane-2,5-diol (1.15 g, 8.97 mmol) and 15-crown-5 (0.054 mL, 0.269 mmol) in tetrahydrofuran (30.0 mL, 8.97 mmol) were added at 10 °C (ice/water bath) finely ground sodium hydroxide (2.15 g, 53.8 mmol) and l-(bromomethyI)benzene (1.07 mL, 8.97 mmol). After stirring at 10 °C for 3 h, the mixture was stirred at ambient temperature overnight. The mixture was partitioned between EtOAc and water, and the organic portions were washed with brine, and cone, in vacuo. The crude product was purified by flash column chromatography (0 to 80% of ethyl acetate in hexanes). The title compound was obtained as a colorless oil.
Example 101-(lR,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-one.
[0747] Silica gel 60 (particle size, 0.040-0.063 mm, CAS # 63231 -67-4, from EMD Chemical Inc. 9.0 g) was added to a solution of (lR,2S,4R,5S)-5-(benzyloxy)bicyclo[2.2.1]heptan-2-ol (2.79 g, 12.8 mmol) in anhydrous dichloromethane 101 (60.0ml). The mixture was cooled to 0 °C, and pyridinium chlorochromate (4.40 g, 20.4 mmol) was added. The reaction mixture was warmed to ambient temperature and stirred at this temperature for 5 h. After this time, the mixture was diluted with dichloromethane (60 mL) and then filtered through a pad of Celite. The solvent was removed in vacuo, and the residue was purified by flash column chromatography (0 to 25% of ethyl acetate in hexanes) to give the title compound as a colorless oiL Example 102-(lR,4R,5S)-5-(Benzyloxy)-2,2 difluorobicyclo-[2.2.1]heptane.
[0748] Deoxo-Fluor (50% in THF, 17.7 g, 40.0 mmol) was added to (lR,4R,5S)-5-(benzyloxy)bicyclo[2.2.1]heptan-2-one (2.45 g, 11.3 mmol) in a 250 mL round-bottom flask.
The mixture was heated to 85 °C (oil bath temperature) and stirred at this temperature under nitrogen for 16.5 h. After cooling to ambient temperature, the mixture was diluted with ethyl acetate, then poured into sat'd NaHC03 in ice. The organic portion was separated, washed with brine, dried over MgSC , filtered, and cone, in vacuo. The crude product was purified by flash column chromatography (0 to 5% of ethyl acetate in hexanes) to give the title compound as a colorless oil.
[0749] Palladium (10 wt. % on activated carbon, 0.28 g) was added to a solution of (lR,4R,5S)-5-(benzyloxy)-2,2-difluorobicyclo[2.2.1]-heptane (1.43 g, 6.0 mmol) in methanol (15 mL), and the mixture was placed under a balloon full of hydrogen. After stirring at ambient temperature for 4 h, the mixture was filtered through a pad of Celite, and the filtrate was concentrated in vacuo. The residue was adsorbed onto a small pad of silica gel, and eluted with 20 % of ethyl acetate in hexanes. The solvents were removed in vacuo to give the title compound as a white solid. 102 Example 104-(lR,4R)-5,5-Difluorobicyclo[2.2.1]heptan
[0750] Silica gel 60 (particle size, 0.040-0.063 mm, CAS # 63231 -67-4, from EMD Chemical Inc. 4.0 g) was added to a solution of (lR,2S,4R)-5,5-difluorobicyclo[2.2.1]heptan-2-ol (0.800 g, 5.40 mmol) in anhydrous dichloromethane (20.0ml). The mixture was cooled to 0 °C, and pyridinium chlorochromate (1.86 g, 8.64 mmol) was added. The reaction mixture was warmed to ambient temperature and stirred at this temperature overnight. After this time, the mixture was diluted with dichloromethane (30 mL) and then filtered through a pad of silica gel. Removal of the solvents gave the title compound as a white solid.
Example 105-(lR,2R,4R)-5,5-DifluorobicycIo[2.2.1]heptan-2-oI.
[0751] -To a solution of (lR,4R)-5,5-difluorobicyclo[2.2.1]heptan-2-one (0.540 g, 3.7 mmol) in anhydrous tetrahydrofuran (8.00 mL) at -78 °C under nitrogen was added drop-wise L-Selectride (1.0 M solution in tetrahydrofuran, 7.40 mL). After stirring at -78 °C for 3 h, 30% ¾02 (6.0 mL) and 10% NaOH (aq., 10.0 mL) were added. The mixture was warmed to r.t. and then stirred at 65 °C for 10 h. After cooling to ambient temperature, the mixture was extracted with EtOAc (50 mL x 2). The combined organic portions were washed with "brine, and cone, in vacuo. Flash column chromatography (0 to 30% of ethyl acetate in hexanes) gave the title compound as a white solid. .
Example 106-2-((lR,2S,4R)-5,5-DifIuorobicyclo[2.2.1]heptan-2-yI)isoindoline-l,3-dione.
[0752] A solution of diethyl azodicarboxylate (0.56 mL, 3.6 mmol) in anhydrous THF (3.0 mL) was added drop-wise to a mixture of (lR,2R,4R)-5,5- 103 difluorobicyclo[2.2.1]heptan-2-ol (0.44 g, 3.0 mmol), phthalimide (0.50 g, 3.4 mmol), and triphenyl phosphine (0.78 mL, 3.4 mmol) in anhydrous tetrahydrofuran (15.0 mL) at r.t. under nitrogen. After stirring at ambient temperature for 66 h, the solvents were removed in vacuo. The residue was partitioned between ethyl acetate and water, and the organic portion was separated, washed with brine, and cone, in vacuo. Flash column chromatography (0 to 35% of ethyl acetate in hexanes) gave the title compound as an off-white solid.
Example 107-(lR,2S,4R)-5,5-Difluorobicyclo[2.2.1]heptan-2-amine hydrochloride.
[0753] To a suspension of 2-((lR,2S,4 )-5,5-difluorobicyclo[2.2.1 ]-heptan-2-yl)isoindoline-l,3-dione (0.58g, 2.09 mmol) in ethanol (anhydrous, 30 mL) was added hydrazine (0.10 mL, 3.14 mmol). After refluxing this mixture under nitrogen for 5 h, it was cooled in an ice bath, and hydrochloric acid (37%, 0.50 mL) was added. After stirring at 60 °C for 1.5 h, the mixture was cooled to ambient temperature. After the white solid was removed by filtration, the filter cake was washed with methanol, and the filtrate was cone, in vacuo. The resulting residue was diluted in ~ 50 mL of water, filtered, and the filtrate was washed with diethyl ether (30 mL x 3). The filtrate was then treated with sodium carbonate monohydrate to saturation, and the aqueous layer was extracted with diethyl ether (50 mL x The solution was treated with hydrochloric acid (1M aqueous, 4 mL), stirred for 5 min, and then concentrated in vacuo to give the title compound as a white solid.
Example 108-l-Benzoyl-3-((lR,2S,4R)-5,5-difluorobicyclo-[2.2.1]heptan-2-yl)thiourea.
[0754] Benzoyl isothiocyanate (0.32 mL, 2.34 mmol) was added to the mixture of (lR,2S,4R)-5,5-difluorobicycle [2.2.1] heptan-2-amine hydrochloride (0.33 g, 1.80 mmol) and triethylamine (0.38 mL, 2.70 mmol) in anhydrous chloroform (25.0 mL) at ambient temperature under nitrogen. After stirring overnight, the reaction mixture was concentrated in vacuo. Water (50 mL) was added to the residue, and it was extracted with diethyl ether (2 104 x 50 mL). The organic portions were combined, washed with brine, and cone, in vacuo to give a light yellowish oil as the title compound that was used in the following reaction without purification. Mass Spec m/z: 311.1 (M+H)+.
Example 109-1 -((lR,2S,4R)-555-difluorobicyclo [2.2.1 ] heptan-2-yl)th ibu rea.
[0756] A mixture of l-benzoyl-3-((lR,2S,4R)-5,5-difluorobicyclo-[2.2.1]heptan-2-yl)thiourea (~ 1.80 mmol) and potassium carbonate (1.49 g, 10.8 mmol) in methanol ( 5.0 mL), water (2.5 mL), and tetrahydrofuran (2.5 mL) was stirred at ambient temperature for 2 h. The reaction mixture was concentrated in vacuo, and the residue was partitioned between EtOAc and water. The organic portion was washed with brine, cone, in vacuo, and purified by flash column chromatography (0 to 65% of ethyl acetate in hexanes) to give the title compound as a white solid. MS m/z: 207.0 (M+H)+.
Example 110-2-(2-ChlorophenyI)-2-methylpropanenitrile.
METHOD R
[0757] A 500 mL round-bottomed flask was charged with 2-(2-chlorophenyl)acetonitrile (6.82 g, 0.045 mol) and 30 mL of THF. This solution was cooled to -40 °C, and KHMDS (0.5 M in toluene, 200 mL, 0.100 mol) was added at such a rate that the internal temperature did not rise above—40 °C. This solution was allowed to stir between -40 to -50 °C for an additional 1 h; After that time, Mel (14.2 g, 6.25' mL, 0.100 mol) was added and the solution was warmed to room temperature (a thick solid formed). The reaction was stirred for 1 h at room temperature then quenched by the addition of saturated aqueous NaHC03. The layers were separated, and the aqueoiis phase was extracted with CH2C12. The combined organic extracts were dried and concentrated in vacuo to give ah oil that was purified by column chromatography (Si02, 100% hexanes to 90% hexanes/ethyl acetate) to provide 2-(2-chlorophenyl)-2-methylpropanenitrile as a colorless oil. 105 Example 111 -2-(2-Chlorophenyl)propan-2-amin e.
[0758] 2-(2-Chlorophenyl)-2-methylpropanenitrile (5.0 g, 0.028 mol) along with 50 mL of EtOH was added into a 250 mL round-bottomed flask. To this was added 50 mL of saturated aqueous K2CO3. This mixture was cooled to 0 °C then 85 mL of 30% aqueous H202 was slowly added. The reaction mixture was allowed to warm to room temperature, and then it was stirred at that temperature for 12 h. The mixture was extracted with CH2CI2 (3 x 150 mL), and the combined organic extracts were dried over MgS04, filtered, and concentrated in vacuo to give a viscous oil. To this oil was added 40 mL of CH3CN, 40 mL H20, and 13.2 g (0.031 mol) of PhI(02CCF3)2. This mixture was stirred at r.t. for 12 h, diluted with 300 mL of H20, and then stirred for an additional 4 h at room temperature. The aqueous phase was extracted using MTBE (1 x 200 mL) follow by diethyl ether (2 x 100 mL). The aqueous layer was basified with IN NaOH (pH =13) and then extracted with CH2CI2 (3 x 100 mL). The organic extracts were dried and concentrated in vacuo to give the desired product as a colorless oil that was used in subsequent steps without further purification.
METHOD S
[0759] To a 50 mL round-bottomed flask was added (l1S',4i?)-bicyclo[2.2.1 Jheptane-2-carboxylic acid (9.84 g, 70 mmol) and bromine (4.10 ml, 80 mmol). The suspension was stirred at room temperature until dissolution. Trichlorophosphine (0.30 ml, 3.4 mmol) was then added slowly and drop wise (significant exotherm observed). A reflux condenser was fitted to the flask with a nitrogen gas inlet and gas outlet (Tygon tubing) running into a scrubber solution of sodium sulfite (l M, 200 mL). After the addition was complete, the reaction mixture was heated in a silicone oil bath at 80 °C for 4 h. After this time, the reaction 106 was cooled to 10 °C and phosphorus-trichloride (4.23 ml, 48.3 mmol) was added drop- wise. The reaction was then heated to 80 °C. During this time the color intensity of the reaction decreased, and after 8 h, the reaction mixture appeared dark orange. The reaction was then cooled to room temperature and diluted with ether (1 L). The ethereal solution was transferred to a separation funnel and washed with 1M sodium sulfite (2 X 500 mL), water (1 X 500 mL), and brine (1 X 500 mL). The organic layer was dried over MgSO.4, filtered, and concentrated in vacUo to afford an oil. Ice cold pentane (50 mL) was then added to the crude product, and the mixture was stirred vigorously. After 20 min, a fine white precipitate formed, which was filtered and washed with pentane (20 mL) and then air dried under a gentle vacuum to afford (4S)-2-bromobicyclo[2.2.1]heptane-l-carboxylic acid (100.2 g, 457 mmol) as a white solid material.
Example 113-Bicyclo|2.2.1]heptane-l-carboxylic acid.
[0760] A 2-L reactor equipped with an overhead mechanical stirrer, condenser, nitrogen gas inlet port, temperature probe and reagent charging port, was placed under an . atmosphere of nitrogen. The reactor was charged with zinc powder (<10 micron) (298 g, 4560 mmol) and acetic acid (500 mL). While vigorously stirring the heterogeneous mixture, (4S)-2-bromobicyclo[2.2.1]heptane-l-carboxylic acid (100 g, 456 mmol) was then added. A second portion of acetic acid (500 mL) was then used to rinse the walls of the reactor. The reaction mixture was brought to a gentle reflux (ca. 30 min) and then held at this temperature for 5 h. The cooled (room temperature) reaction mixture was passed through a pad of Celite, which was washed with acetic acid (1 X 300 mL) and ethyl acetate (1 ( 500 mL). The filtrate was concentrated, water (300 mL) was added, and then the mixture was stirred vigorously to induce precipitation. The precipitate was collected by filtration, washed with water, and dried under vacuum at 35 °C overnight. Pentane (50 mL) was then added, and the mixture was stirred vigorously for 20 in during which time a fine white precipitate formed. The resulting. precipitate was filtered, washed with pentane (20 mL), and air dried to afford bicyclo[2.2.1]heptane-l-carboxylic acid (52 g) as a white solid. 107 Example 114-ieri-Butyl bicyclo[2.2.1]heptan-l-yIcarbamate.
NHtBoc
[0761] A 100 mL round-bottomed flask equipped with a condenser and nitrogen inlet was charged with bicyclo[2.2.1]heptane-l-carboxylic acid (2.00 g, 14.3 mmol), toluene (35 mL), triethylamine (2.18 ml, 15.7 mmol) and diphenylphosphoryl azide (3.38 ml, 15.7 mmol) at room temperature under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature for 1 h before being heated to 50 °C for 3 h. Gas evolved from the reaction mixture for approximately 2-3 h. After 3 h at 50 °C, the temperature of the reaction mixture was increased to 70 °C and stirring continued for another 2 h until no further gas evolution occurred. The reaction mixture was then cooled and thenxoncentrated in vacuo. The resulting oil was dissolved in anhydrous t-BuOH (10 mL, 99.9% anhydrous packed under argon; Alfa Aesar), placed under and atmosphere of nitrogen, and refluxed in a 90 °C bath for 14 h. After this time, the reaction mixture was cooled and concentrated under reduced pressure to afford an off-white solid which was then dissolved in ether (50 mL), washed with water (20 mL), 1M NaOH (20 mL), water (20 mL) and brine (20 mL). After being dried over MgS04, the mixture was filtered and concentrated in vacuo to afford 2.2 g of an off-white solid. Pentane (20 mL) was added, and solution was stirred vigorously until dissolve was removed through a fine grade sintered glass filter funnel. The mother liquor was concentrated to afford the title compound (2.2 g) as an off white solid.
Example 115-l-(Bicyclo[2.2.1]heptan-l-yl)thiourea.
[0762] A 100 mL RBF was purged with nitrogen gas before being charged with tert-butyl bicyclo[2.2.1]heptan-l-ylcarbamate (6.60 g, 31.0 mmol) and dichloromethane (66 mL). The solution was cooled in a 0 °C a bath, and then trifluoroacetic acid (12 mL, 18 g, 156 mL) was added. The cooling bath was removed, and the reaction mixture was allowed to warm to room temperature during which time a gas evolved from the reaction mixture. After 3 h at room temperature the reaction mixture was concentrated in vacuo to afford a viscous oil. 108 This material was dissolved in dichloromethane (82 mL), and triethylamine (13.0 mL, 94 mmol) and benzoyl isothiocyanate (4.6 mL, 34 mmol) were added. After stirring at room temperature under an atmosphere of nitrogen for 14 h, the reaction mixture was concentrated in vacuo, and the resulting residue was dissolved in MeOH/THF/¾0 (2 : 1 : 1 , ca. 0.3 M). Potassium carbonate (22 g, 156 mmol) was added, and the biphasic solution was vigorously stirred for 3 h. The organic solvents were removed under reduced pressure during which time a yellow precipitate formed. The precipitate was filtered, washed with water (30 ml) and cold (-20 °C) diethyl ether to provide a white precipitate. This material was allowed to air dry for 10 min and then dried under high vacuum at room temperature for ca. 18 h to afford the title compound (3.8 g) as a fine white powder.
Example 116- 4-(2-(4-MethyI-3-nitrophenoxy)ethyl)morpholine.
METHOD T
[0763] A mixture of 4-methyl-3-nitrophenol (1.53 g, 10 mmol.), 4-(2-chloroethyl)morpholine (2.79 g, 15 mmol), Cs2C03 (9.78 g, 30 mmol) and Nal (145 mg, 1 mmol) in DMF (15 mL) was stirred for 3 h at 80 °C. The reaction mixture was then cooled to room temperature, diluted with water, and extracted with EtOAc. The organic layer was dried over MgSC>4, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1:0.05 CH2Cl2/EtOAc/MeOH) to give the title compound as an oil.
Example 117-2-Methyl-5-(2-morpholinoethoxy)benzenamine.
[0764] To the mixture of 4-(2-(4-methyl-3-nitrophenoxy)ethyl)morpholine (532 mg, 2 mmol) in MeOH (50 mL) was added 10% Pd/C (250 mg). The mixture was stirred under an atmosphere of ¾ (balloon) overnight. The contents of the reaction mixture were then filtered and concentrated in vacuo to give the title product, which was used without further purification. 109 Example 118-l-(2-Chlorophenyl)cyclopropanamine.
[0766] METHOD U
[0767] This compound was prepared using the method described by Bertus and Szymoniak; J. Org. Chem. 2003, 68, 7133.
Example 119-tert-Butyl 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-ylcarbamate.
METHOD V
[0768] To a flame-dried 100 mL round-bottomed flask equipped with magnetic stirring and argon inlet/outlet was added 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octane-l-carboxylic acid (200 mg, 649 μιηοΐ, prepared by the method described in US Patent Application: 2004/0133011 and 5 mL of toluene. Triethylamine (0.10 mL, 713 μπιοΐ) was warmed in a 50 °C oil bath for 30 min, then to 70 °C for 5 h. terr-Butanol (5 mL, 53 mmol) was then added, and the reaction mixture continued to stir in the 70 °C bath. After 20 h, copper (I) chloride (10 mg, 101 μπιοΐ) was added, and the reaction continued to stir for ca 1.5 d at 70 °C. The reaction was removed from the oil bath and then poured thru a 1 cm pad of Celite. The Celite pad was washed with CH2C12, and the filtrate was concentrated in vacuo. CH2C12 (50 mL) was added to the filtrate, and the organic layer was washed with 1M NaOH (2x), sat'd NH4CI, sat'd NaHC03, and brine. The organic layer was then dried over MgS04, filtered and concentrated in vacuo to give fe?-t-butyl 4-(4- (methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-ylcarbamate (mass = 170 mg). The crude reaction product was taken onto the next step without further purification. 110 Example 120-4-(4-(Methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-amine.
[0769] To a 100 mL round-bottomed flask equipped with magnetic stirring was added tert-butyl 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-ylcarbamate (170 mg, 448 μπιοΐ), 2 mL of CH2C12, ca. 5 drops of water, and trifluoroacetic acid (2 mL, 27 mmol). The reaction mixture was stirred at ambient temperature for 3.5 h, after which time the mixture was concentrated in vacuo. NaOH (ca. 50 mL of a 1M aq. solution) was added to the mixture, and the aqueous layer was extracted with CH2C12 (3 x 15 mL). The organic layers were combined, dried over K2C03, filtered, and concentrated in vacuo to give 4-(4-(methylsulfonyl)phenyl)bicycld[2.2.2]octan-l-amine (mass = 120 mg, Mass Spec, m/z + ion = 280.2) The crude reaction product was taken onto the next step without further purification.
Example 121-l-BenzoyI-3-(4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-yI)thiourea.
[0770] To a 100 mL round-bottomed flask equipped with magnetic stirring was added 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-amine (120 mg, 429 μπιοΐ) in 2 mL of CH2C12, and benzoyl isothiocyanate (63.6 μΐ, 472 μπιοΐ). The reaction was stirred at ambient temperature for ca. 26 h, and then it was concentrated in vacuo to give l-benzoyl-3-(4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-yl)thiourea (mass = 185 mg, Mass spec. m/z + ion = 443.2). The crude reaction product was taken onto the next step without further purification.
I l l Example 122-l-(4-(4-(MethylsuIfonyI)phenyl)bicyclo[2.2.2]octan-l-yI)thiourea.
[0771] To a 100 mL round-bottomed flask equipped with magnetic stirring was added a solution of l-benzoyl-3-(4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-yl)thiourea (185 mg, 418 μιηοι) suspended in THF (1.5 mL) and methanol (3 mL). A solution of potassium carbonate (289 mg, 2090 μπιοΐ) in 1.5 mL of water was added, and the reaction mixture was stirred at ambient temperature. After 3.5 h, 3 mL more of THF was added. Then after 22.5 h, the lower boiling solvents of the reaction mixture were removed in vacuo. Water was added, and the aqueous layer was extracted with EtOAc (1 10 mL), CH2C12 (3 x 10 mL), and EtOAc (1 x 20 mL). The aqueous layer was the saturated with solid NaCl, and it was extracted with THF (3 10 mL). All organic layers were combined along with 30 mL more THF and dried over K2C03, filtered, and concentrated in vacuo. The residue was absorbed onto silica gel and purified on a 40 g silica gel column using 1 :2 hexanes-EtOAc + 2% MeOH as the eluant followed by 1:2 hexanes-EtOAc + 4.5% MeOH. Purified l-(4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-l-yl)thiourea was isolated from Example 123-Bicyclo[2.2.1]heptane-2-carboxamide.
METHOD W
[0772] A round-bottomed flask was charged with 450 g exo-2-norbornyl carboxylic acid (3200 mmol) in 100 mL of CH2C12. To the solution was added 0.23 mL of DMF (3.21 mmol) followed by the drop-wise addition of 325 mL of oxalyl chloride (3700 mmol). The reaction was stirred for 1 h at ambient temperature then warmed to 45 °C for an additional 30 min. The reaction was allowed to cool to ambient temperature and 2.5 L of 28 % NH4OH 112 was slowly added. The reaction was stirred for 1 h at ambient temperature. The desired product was isolated by filtration.
Example 124-l-Benzoyl-3-(bicyclo[2.2.1]heptan-2-ylmethyl)thiourea.
[0773] A dry 500 mL round-bottomed flask equipped with a magnetic stir bar under an atmosphere of N2 was charged with 3.96 g (28.5 mmol) of bicyclo[2.2.1]heptane-2-carboxamide in 30 mL of anhydrous THF. The mixture was cooled to 0 °C and 57 mL (57 mmol) of lithium aluminum hydride (1.0 M in THF) were added via syringe. The reaction was stirred for 10 min. at 0 °C then allowed to warm to ambient temperature and stirred an additional 15 h. The reaction solution was then cooled to 0 °C, and 2.2 mL of H20 were added drop-wise followed by the addition of 2.2 mL of 15% aq. NaOH. Water (6.6 mL) was then added and the reaction was allowed to stir for 0.5 h at ambient temperature. The solids were removed by filtration through a Celite pad. Trifluoroacetic acid (2.6 mL) was then added to the filtrate, and the mixture stirred for 1 h at ambient temperature. The solvent was removed in vacuo providing amine salt as a white solid.
[0774] A dry 150 mL round-bottomed flask equipped with a magnetic stir bar under an atmosphere of N2 was charged with 5.46 g (22.8 mmol) of amine salt in 50 mL of C¾C12. To the solution was added 6.5 mL (46.6 mmol) of triethylamine followed by the drop-wise addition of 3.05 mL (22.7 mmol) of benzoyl isothiocyanate. After stirring the reaction mixture for 1.3 h at ambient temperature, the organic layer was washed with H20 (2 x 25 mL), 1M KOH (2 x 25 mL), 1M HC1 (2 x 25 mL), and brine. The organic phase was dried over MgS0 , filtered, and concentrated in vacuo to provide the desired N-acylthiourea. MS (ESI, pos. ion) m/z: 289.2 (M+H).
Example 125-l-(Bicyclo[2.2.1]heptan-2-ylmethyl)thiourea. 113 2 05/018081
[0775] A 250 mL round-bottomed flask equipped with a magnetic stir bar was charged with 6.17 g (22.4 mmol) of l-benzoyl-3-(bicyclo[2.2.1]heptan-2-ylmethyl)thiourea in 30 mL of MeOH. KOH was added (2.55 g, 45.4 mmol) and the reaction was stirred at ambient temperature for 4 h. Water (Γ50 mL) was then added to the reaction mixture, and the solid was removed by filtration. The flask and filter cake were rinsed with 40 mL of H20. The collected solid was then suspended in 15 mL of MTBE, and the solid was collected by filtration providing the desired thiourea. MS (ESI, pos. ion) m/z: 185.2 (M+H).
Synthesis of Final Products, (procedures: METHOD-X, METHOD-Y, METHOD-Z, METHOD-AA, METHOD-BB, METHOD-CC, METHOD-DD, METHOD-EE, METHOD-FF, METHOD-GG, METHOD-II, METHOD-JJ, METHOD-KK, METHOD-LL METHOD-MM, METHOD-NN, METHOD-OO, METHOD-PP).
Example 126-6-(Cycloheptylamino)-5-thia-7-azaspiro[3.4)oct-6-en-8-one.
METHOD X
[0776] A mixture of 1-cycloheptylthiourea (0.255 g, 1.48 mmol) and ethyl 1-bromocyclobutanecarboxylate (0.25 mL, 1.48 mmol, Aldrich) in N,N-diisopropylethylamine Optimizer from Personal Chemistry) at 155 °C for 2 h, then at 170 °C for 1.5 h. After removing the low-boiling solvents in vacuo, the residue was partitioned between EtOAc and water. The organic portion was separated, washed with brine, and cone, in vacuo. The residue was purified by flash column chromatography (0 to 35% of EtOAc in hexanes) 'to give the title compound as a tan solid. MS m/z: 253.2 (M+H)+ Example 127-Ethyl 4-oxo-2-(2-(trifluoromethyI)phenyIaniino)-4,5-dihydrothiazole-5-carboxylate. 114 METHOD X
[0777] To a stirred solution of 2-(trifluoromethyl)phenylthiourea (Menai Organics, 2.36 g, 10.7 mmol), Hunig's base (Aldrich, 1.9 mL, 10.7 mmol) in EtOH (10 mL) was added diethyl bromomalonate (2.0 mL, 10.7 mmol). After 1.5 h at room temperature, the reaction mixture was diluted with EtOAc, washed with saturated NaHC03 and brine, dried over Na2S04, filtered, and concentrated in vacuo, The crude product was purified by silica gel chromatography. MS: 333 (M+l).
Example 128-(5i?)-(±)-ei7i -2-(BicycIo[2.2.1]heptan-2-yIamino)-5-isopropylthiazoI-4(5H)-one.
METHOD Y
[0778] To a stirred solution of (±)-endo-\ -(bicyclo[2.2. l]heptan-2-yl)thiourea (314 mg, 1.84 mmol) and (5)-2-bromo-3-methylbutanoic acid (334 mg, 1.84 mmol) in anhydrous ethariol (10 mL) under nitrogen, was added sodium acetate (182 mg, 2.21 mmol, 1.2 equ.) at room temperature. After refluxing the reaction mixture for 3 h, the solvent was evaporated in vacuo, and the residue was taken up in ethyl acetate (20 mL). The organic layer was washed with water (20 mL) followed by brine (20 mL), then dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (Si02 4: 1 hexane/acetone) to afford the title compound (90 mg). MS (ESI, pos. ion) m/z: 253.1 (M+H).
Example 129 5)-2-((re lJ?,2i?,45)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazoI-4(5H)-one.
METHOD Z 115 1
[0779] To a solution of (J?)-2-bromo-3-methylbutanoyl isothiocyanate (734 mg, 3.30 mmol) in CH2C1 at 0 °C was added drop-wise _u'0-2-aminonorbornane (0.4 mL, 3.37 mmol). The mixture was allowed to stir for 30 min at 0 °C. Triethylamine (0.47 mL, 3.38 mmol, 1.02 equiv) was then added, and the mixture allowed to warm to room temperature and stirred overnight. The mixture was concentrated and the resulting oil triturated with THF (26 mL), filtered, and concentrated in vacuo. Flash chromatography (gradient of hexanesracetone gradient - automated, hexanes.acetone 4:1 - manual) furnished the title compound as a sticky white solid. Material was foamed by dissolution in CH2CI2 followed by re-concentration.
Example 130-5 sopropyl-5-methyl-2-(pyridin-2-ylmethylarnino)thiazol-4(5jH)- ne.
METHOD Z
[0780] Pyridin-2-ylmethanamine (0.22 mL, 2.1 mmol) was added to 2-bromo-2,3-dimethylbutanoyl isothiocyanate (240 mg, 1.1 mmol) at room temperature. The reaction was exothermic, and was stirred at room temperature for 15 min. CH2C12 (2 ml) was added, and the resulting precipitate was removed by filtration. The CH2C12 solution was concentrated, (10% NH3 in MeOH) in CH2C12) to give the title compound as an off-white solid (123 mg). Mass Spec. = m/z + ion 264.1 (M+H) Example 131-5-Cyclopentyl-5-fluoro-2-(2-fluorophenylamino)thiazol-4(5H)-one.
METHOD BB
[0781] A dry 100 mL round-bottomed flask was charged with 5-cyclopentyl-2-(2-fluorophenylamino)thiazol-4(5H)-one (0.200 g, 0.717 mmol) and 6.0 mL of THF. This solution was cooled to -78 °C, and LDA (2.0 M in THF/heptane/ethyl benzene, 1.43 mL, 116 2.86 mmol) was added. The resulting brown solution was allowed to stir at that temperature for 1 h, then TMSC1 (0.623 g, 0.725 mL, 5.74 mmol) was added. The solution was warmed to room temperature and allowed to stir for an additional 1 h. The solution was concentrated in vacuo to remove the volatiles and then redissolved in 10 mL of C¾CN. Selectfluor® (0.508 g, 1.43 mmol) was added at room temperature, and the resulting solution was stirred for 2 h. The reaction was quenched with saturated aqueous NaHC03, and the resulting mixture was thoroughly extracted with CH2C12. This combined organic extracts were dried and concentrated in vacuo to give an oil which was purified by column chromatography (100% to 70% hexanes/30% ethyl acetate) to give the title compound as a colorless oil. Mass Spec (M+H)+; 297.1.
Example 132-2-(Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(trifluoromethyl)thiazoI-4(5J9)-one.
METHOD CC
[0782] A dry 100 mL round-bottomed flask equipped with a magnetic stir bar under an atmosphere of N2 was charged with 528 mg (2.35 mmol) of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one in 5 mL of anhydrous THF. The reaction was cooled to -20 °C and 5.0 mL (5.0 mmol) of NaHMDS (1.0M in THF) were added drop-wise via syringe. The resulting reaction mixture was stirred at -20 °C for 30 min then 0.86 mL (6.78 mmol) of TMSC1 was added drop-wise via syringe. The reaction mixture was held at -20 °C for 15 min, and then the mixture was allowed to warm to ambient temperature. After stirring the reaction mixture for an additional 1 h, the mixture was concentrated in vacuo. The reaction flask was again equipped with a magnetic stir bar and placed under an N2 atmosphere. Anhydrous C¾CN was added, and 978 mg (2.58 mmol) of S-(trifluoromefhyl)dibenzothiophenium-3-sulfonate C2H5OH was added to the reaction mixture in one portion, and the resulting suspension was stirred at ambient temperature for 19 h. The solids were then removed by filtration through a Celite pad, and the reaction flask and pad were rinsed with CH2C12. The organic layer was washed with 20 mL of 1 : 1 H20/sat'd NH4C1, and the aqueous layer was extracted with an additional portion of CH2C12. The 117 combined organic layers were washed with brine, dried over MgS04, filtered, and concentrated in vacuo. Flash chromatography (Si02, CH2C12 to 5% MeOH/CH2Cl2) provided the desired compound. MS (ESI, pos. ion) m/z: 293.1 (M+H).
Example 133-Ethyl 5-(3-tert-butoxy-3-oxopropyl)-4-oxo-2-(2-(trifluoromethyl)phenylamino)-4,5-dihydrothiazole-S-carboxylate.
METHOD DD
[0783] The above compounds were prepared according to the procedure reported in the literature: see S. Muthusamy Synth. Commun. 2002, 32, 3247. To a stirred solution of ethyl 4-oxo-2-(2-(trifluoromethyI)phenylamino)-4,5-dihydrothiazoIe-5-carboxyIate (1.1 g, 3.3 mol), iert-butyl acrylate (Aldrich, 2.5 mL, 16.5 mmol) in EtOH (10 mL) was added D3U (Aldrich, 0.25 mL, 1.6 mmol). The mixture was stirred at r.t. overnight and concentrated in vacuo. The crude product was purified by silica gel chromatography. MS: 461 (M+l).
Example 134-ferf-Butyl 3-(4-oxo-2-(2-(trifluoromethyl)phenylamino)-4,5-dihydrothiazoI-5-yl)propanoate.
[0784] To a mixture of ethyl 5-(3-tert-butoxy-3-oxopropyl)-4-oxo-2-(2-(trifiuoromethyl)phenylamino)-4,5-dihydrothiazole-5-carboxylate (88.7 mg, 0.19 mmol), THF (1 mL), MeOH (0.3 mL), and water (0.3 mL) was added LiOH-H20 (Aldrich, 20 mg, 0.47 mmol) at room temperature. After 3 h, IN HC1 (0.7 mL) was added to the reaction mixture at 0 °C. The mixture was extracted with EtOAc, and the organic phase was dried over Na2S04, filtered, and concentrated in vacuo. The crude material was purified by silica gel chromatography. MS: 389 (M+l). 118 Example 135-2-((1 ,25,4i?)-Bicyclo[2.2.1]hept-2-ylamino)-8-oxa-l-thia-3-azaspiro[4.5]dec-2-en-4-one.
METHOD
[0785] To the mixture of 2-((15',25,4i?)-bicyclo[2.2.1]heptan-2-ylamino)thiazoI-4(5H)-one (840 mg, 4.0 mmol) in THF (5.0 mL) was added LDA (2.0 M, 20 mL) at -78°C. The resulting mixture was stirred for 10 min at -78°C, and then l-bromo-2-(2-bromoethoxy)ethane (3.71 g, 16 mmol) was added. The mixture was allowed to warm to room temperature and then stirred overnight. A sat'd solution of NaH2P04 was added, and it was extracted with EtOAc. The organic layer was washed with sat'd NH4C1, dried over MgSC , filtered, and concentrated in vacuo. The crude residue was purified through flash chromatography (4: 1 :0.05; CH2Cl2/EtOAc/MeOH) to give the title compound as off-white solid. MS (ES+): 281 (M+H)+.
Example 136-2-((15 25;4j¾-BicycIo[2.2.1]heptan-2-ylamino)-5-(2-hydroxypropan-2-yl)-5-methylthiazoI-4(5H)-one.
METHOD FF
[0786] To a solution of 2-((l S,2S,4i?)-bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one (1.10 g, 5.0 mmol) in THF (5 ml) at -78 °C was added LDA (2.0 M, 10 ml). After 5 min, acetone was added; and the reaction mixture was stirred for 1 h at -78°C. The resulting reaction mixture was poured into a sat'd NaH2P04, and extracted with EtOAc. The organic layer was dried over MgS04, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title 119 compound as a white solid. MS (ES+): 283 (M+H)+. The diastereomers were separated using standard HPLC methods described within this text.
Example 137-2-((15,25,4i¾)-Bicyclo[2.2.1]heptan-2-ylarnmo)-5-(2-fluoropropan-2-yl)-5-methylthiazol-4(5H)-one.
METHOD GG
[0787] To the solution of DAST (527 mg, 3.3 mmol) in CH2C12 (2 ml) at -78 °C was added a solution of 2-((liS')2-S,,4i?)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxypropan-2-yl)-5-methylthiazol-4(5H)-one in CH2C12 (8 ml) over 10 min. After the addition, the cold bath was removed and the temperature was allowed to warm up to 0 °C, and then quenched with sat'd NaHC03. The mixture was extracted with CH2CI2, dried over Na2S04, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as white solid. MS (ES+): 285 (M+H)+. The diastereomers were separated using standard HPLC methods described within this text.
Example 138-5-Isopropyl-5-methoxy-2-(tricyclo[3.3.1.13,7]decan-l-ylamino)-thiazol-4- METHOD II
[0788] A mixture of 5-(l-methylethyl)-2-(tricyclo[3.3.1.13,7]dec-l-ylamino)-l,3-thiazol-4(5H)-one (146 mg, 0.5 mmol) and NBS (107 mg, 0.6 mmol) in CC14 (60 mL)was stirred at reflux for 30 min. The resulting mixture was cooled to 0 °C, and filtered to remove the solid. The residue was then concentrated in vacuo and diluted with CH2C12 (20 mL). To this mixture was added MeOH (200 uL) and DIEA (200 uL). The mixture was stirred for 30 120 min, then was concentrated in vacuo and purified by flash chromatography (4:1 ; Hexane:EtOAc) to give the title compound as white solid. MS (ES+): 323 (M+H)+.
Example 139-2-(2-(l-Adamantylamino)-4-oxo-4,5-dihydrothiazoI-5-yl)acetaldehyde METHOD JJ
[0789] A suspension of 2-(l -adamantylamino)-5-(2-hydroxyethyl)thiazol-4(5H)-one (0.25 g, 0.85 mmol) in CH2C12(10 mL)was added to Dess-Martin periodinane (0.56 g, 1.28 mmol, Aldrich) in CH2C12(10 mL). After stirring at ambient temperature for 1 h, the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and saturated aqueous sodium thiosulfate and aqueous sodium bicarbonate. The organic portion was separated, washed with brine, and cone, in vacuo to give the title compound as a light yellowish solid. MS m/z: 293.6 (M+H)+.
Example 140-2-((15,25 4R)-bicycIo[2.2.1]heptan-2-ylamino)-5-(2-hydroxyethyl)thiazol-4(5J?)-one.
METHOD KK
[0790] l-((lS,2-S'54i?)-Bicyclo[2.2.1]heptan-2-yl)thiourea (887 mg, 5.25 mmol), 3-bromo-dihydrofuran-2(3H)-one (1.65 g, 5mmol), EtOH (10 mL) and DIEA (5.0 mL) were placed in a microwave reaction vessel. The mixture was placed in a microwave synthesizer and was irradiated at 150°C for 30 min. The resulting mixture was poured into water and extracted with EtOAc and dried over MgS04. After being filtered and concentrated in vacuo, the title compound was obtained a brown solid. MS (ES+): 255 (M+H)+. 121 Example 141-2-((15,25,4J?)-Bicyclo[2.2.1]heptan-2-ylarnino)-5-(2-(tetrahydr pyran-2-yIoxy)ethyI)thiazoI-4(5H)-one
[0791] The mixture of 2-((lS,2_?,4 ?)-bicyclo[2.2. l]heptan-2-ylamino)-5-(2-hydroxyethyl)thiazol-4(5H)-one (3.2 g, 12.6 mmol) and p-toulenesulfonic acid (500 mg) in 3,4-dihydro-2 /-pyran (10 mL) was stirred for 2 h at room temperature. The resulting mixture was diluted with CH2C12 (100 mL), then washed with sat'd NaKbPC , and dried over MgS04. After being filtered and concentrated in vacuo, the crude residue was purified by flash chromatography (3 :2; Hexane-.EtOAc) to give the title compound as an oil. MS (ES+): 339 (M+H)+.
Example 142-2-((15,25,4i?)-BicycIo[2.2.1]heptan-2-ylamino)-5-(2-rnethylanyI)-5-(2-(tetr ahy d ro-2 H-p y r an-2-y loxy)ethyI)thiazol-4(5i_?)-on e.
[0792] To the mixture of 2-((15,25,4/?)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)thiazol-4(5H)-one (1160 mg, 3.43 mmol) in THF (8.0 mL) cooled in a -78°C bath was added LDA (2.0 M, 17.15 mL). The resulting mixture was stirred for 10 min at -78 °C, and then 3-bromo-2-methylprop-l-ene (1.6 ml, 17.15 mmol) was added. After the reaction mixture was allowed to warm to room temperature and stirred ca. 18 h. Saturated NaH2PC>4 was added, and the aqueous phase was extracted with EtOAc. The organic layer was washed with sat'd NH4C1, dried over MgS04, filtered, and concentrated in 122 vacuo. The crude residue was purified by flash chromatography (4: 1 ; Hexane:EtOAc) to give the title compound as yellow oil. MS (ES+): 393 (M+H)+.
Example 143-2-((l-9,25,4ii)-Bicyclo[2.2.1]heptaii-2-ylamino)-5-(2-hydroxyethyl)-5-(2-methylallyl)thiazol-4(5H)-one
[0793] The mixture of 2-((lS,25,,4i?)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-methylallyl)-5-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)thiazol-4(5H)-one (420 mg, 1.07 mmol) and p-toluenesulfonic acid (100 mg) in MeOH (5.0 mL) was stirred for 16 h at room temperature. The reaction mixture was then concentrated in vacuo, and sat'd NaH2P04 was added. The mixture was then extracted with EtOAc, and the organic layer was washed with sat'd NE Cl, dried over MgS0 , filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane: EtOAc) to give the title compound as solid. MS (ES+): 309 (M+H)+.
Example 144-2-((1 2S,4i?)-Bicyclo[2.2.1]hept-2-ylamino)-7,7-dimethyl-8-oxa-l-thia-3-azaspiro[4.5Jdec-2-en-4-one.
[0794] To a solution of 2-((l.?,25,,4/?)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxyethyl)-5-(2-methylallyl)thiazol-4(5H)-one (120 mg) in CH2C12 (3 mL) was added concentrated H2SO4 (200 uL). The resulting mixture was stirred for 16 h, then concentrated in vacuo. The residue was treated with sat'd Na¾PO4 and extracted with CH2C12. The organic layer was washed with sat'd HUCl, dried over MgSO4, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4: 1 ; Hexane:EtOAc) to give 123 the title compound as solid. MS (ES*): 309 (M+H)+. The diastereomers were separated using standard HPLC methods described within this text.
Example 145-2-(Bicyclo[2.2.1]heptan-2-ylamino)-5-(2-(i'e/--'-butyldimethylsilyloxy)ethyi)thiazol-4(5J3)-one.
METHOD LL
[0795] The title compound was prepared according to the procedure described in the preparation of te/-t-butyl 4-((2-((25)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-l-carboxylate by using 2-(bicyclo [2.2.1 ]heptan-2-ylamino)thiazol-4(5H)-one (1 -00 g» 4.76 mmol), lithium diisopropylamide (Aldrich, 2.0 M in heptane/THF/ethylbenzene, 8.5 mL, 19.0 mmol), and (2-bromoethoxy)(ter£-butyl)dimethylsilane (Aldrich, 6.83 g, 28.5 mmol). The title compound was obtained as an off-white solid (950 mg). MS (ESI, pos. ion) m/z: 369 (M+H).
Example 146-2-(Bicyclo[2.2.1]heptan-2-ylamino)-5,5-/i> $(2-(ier/'-hiitv!dimethvlsilv!oxv^ethvl¼hiazol-4f5HVone.
[0796] The title compound was prepared according to the procedure described in the preparation of ter/-butyl 4-((2-((2lS)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-l-carboxylate by using 2-(bicycIo[2.2.1]heptan-2-ylamino)-5-(2-(tert-butyldimethylsilyloxy)ethyl)thiazol-4(5H)-one (630 mg, 1.71 mmol), lithium diisopropylamide (Aldrich, 2.0 M in heptane/THF/ethylbenzene, 4.27 mL, 8.55 mmol), and (2-bromoethoxy)(½rt-butyl)dimethylsilane (Aldrich, 2.46 g, 10.25 mmol). The title compound was obtained as a sticky orange solid (771 mg). MS (ESI, pos. ion) m/z: 413 (M-TBDMS+2H). 124 Example 147-2-(Bicyclo[2.2 ]heptan-2-yIamino)-5,5-bis(2-hydroXyethyl)thiazol-4(5H)-one.
[0797] A mixture of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5,5-bis(2-(¾/-/-butyldimethylsilyloxy)ethyl)thiazol-4(5H)-one (771 mg, 1.46 mmol) in 15 mL of a 1% HCl solution in ethanol was stirred at room temperature for 3 h. The reaction mixture was then concentrated in vacuo. Flash column chromatography (silica gel, 0-8 % MeOH-CH2Cl2) afforded the title compound as a colorless thin film (390 mg). MS (ESI, pos. ion) m/z: 299 (M+H).
Example i48-Methanesulfonic acid 2-[2-(bicycIo[2.2.1]hept-2-ylamino)-5-(2-methanesulfonyloxy-ethyl)-4-oxo-4,5-dihydro-thiazol-5-yl]-ethyl ester.
[0798] To a mixture of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5,5-bis(2-hydroxyethyl)thiazol-4(5H)-one (280 mg, 0.94 mmol) and diisopropylethylamine (Aldrich, 412 mg, 3.19 mmol) in CH2C12 (5 mL) was added methanesulfonyl chloride (344 mg, 3.00 mmol, 3.2 eq), and the reaction mixture was stirred at room temperature for 18 h. The reaction mixture was then concentrated in vacuo to provide the title compound which was used without further purification. MS (ESI, pos. ion) m/z: 455 (M+H). 125 Example 149-2-(Bicyclo[2.2.1]hept-2-ylamino)-8-cyclopeiityI-l-thia-3,8-diaza-spiro[4.5]dec-2-en-4-one.
[0799] A mixture of methanesulfonic acid 2-[2-(bicyclo[2.2.1]hept-2-ylamino)-5-(2-methanesulfonyloxy-ethyl)-4-oxo-4,5Tdihydro-thiazol-5-yl]-ethyl ester (half of the crude product from above) and cyclopentylamine (799 mg, 9.38 mmol) in CH2C12 (1.5 mL) was stirred at room temperature for 4 d. Flash column chromatography (silica gel, 0-10 % MeOH in CH2C12) afforded the title compound as an off-white solid (52 mg). MS (ESI, pos. ion) m/z: 348 (M+H).
Example 150-tert-Butyl 4-((2-((25)-bicycIo[2.2.1]Iieptan-2-yIamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yI)methyl)piperidine-l-carboxylate METHOD AA
[0800] To a solution of 2-((2S)-bicyclo[2.2.1 ]heptan-2-ylamino)-5-methylthiazol-4(5H)-one in anhydrous THF (30 mL) at -78 °C under N2 was added lithium diisopropylamide (Aldrich, 2.0 M in heptane/THF/ethylbenzene, 9.2 mL, 18.4 mmol). After stirring the reaction mixture at -78 °C for 1 h, a solution of 4-bromomethyl-piperidine-l-carboxylic acid teri-butyl ester (Pharma Core, 5.12 g, 18.4 mmol, 4.0 eq) in anhydrous THF (10 mL) was added under N2. The resulting reaction mixture was stirred at -78 °C for 4 h. The cooling bath was removed, and the reaction mixture was stirred at ambient temperature for ca. 18 h. Saturated NH4C1 was then added, and the THF was removed in vacuo. The residue was extracted with EtOAc (3 x 180 mL), and the combined organic layers were 126 washed with saturated NaCl, dried over Na2S04, filtered, and concentrated in vacuo. Flash column chromatography (silica gel, 0-60% EtOAc in hexane) afforded the title compound as an off-white solid (1.42 g). MS (ESI, neg. ion) m/z: 420 (M-H).
Example 151-2-((25)-Bicyclo[2.2.1]heptan-2-ylamino)-5-met yi-5-(piperidin-4-ylmethyl)thiazoI-4(5H)-one METHOD MM
[0801] A mixture of iert-butyl 4-((2-((2->)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-l-carboxylate (1.42 g, 3.37 mmol, 1.0 eq) in 50 mL of a 4.7 M HCl solution in EtOAc was stirred at room temperature. After 4 h, the reaction mixture was concentrated in vacuo. Aqueous Na2C03 (2.0 M, 20 mL) was then added, and water was removed in vacuo. The residue was then triturated with 10% Me0H-CH2Cl2 (6 x 100 mL), and the combined triturating solution were concentrated in vacuo. The crude product was dissolved in CH2C12, filtered, and concentrated in vacuo to afford the title compound as a light orange solid (1.08g). MS (ESI, pos. ion) m/z: 322 (M+H).
Example 152-ferf-Butyl 2-(3-(4-((2-((25)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yI)methyl)piperidine-l-carbonyl)phenoxy)ethyIcarbamate
[0802] A mixture of 2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one (534 mg, 1.66 mmol), 4-[2-(Boc-amino)ethyloxy]- 127 benzoic acid (NeoMPS, 701 mg, 2.49 mmol), EDCI (Aldrich, 637 mg, 3.32 mmol, 2.0 eq), HOBt (Aldrich, 45 mg, 0.332 mmol, 0.2 eq) and triethylamine (Aldrich, 336 mg, 3.32 mmol, 2.0 eq) in CH2C12 (10 mL) was stirred at room temperature for ca. 18 h. The reaction was quenched with saturated NaHC03 (100 mL), and the crude product was extracted with C¾C12 (3 x 100 mL). The combined organic extracts were washed with brine, dried over Na2S04, filtered, and concentrated; Flash column chromatography (silica gel, 0-5% MeOH in C¾C12) afforded the title compound as a white solid (800 mg). MS (ESI, pos. ion) m/z: 585 (M+H).
Example 153-5-((l-Acetylpiperidin-4-yI)methyl)-2-((2S)-bicyclo[2.2.1]heptan-2-ylaminoyS-meth lthiazol^iSiiO-one
[0803] A mixture of 2-((25)-bicyclo[2.2.1 ]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one (130 mg, 0.41 mmol), acetic anhydride (Aldrich, 83 mg, 0.81 mmol) and diisopropylethylamine (157 mg, 1.22 mmol) in CH2C12 (3 mL) was with CH2C12 (4 x 60 mL). The combined organic extracts were washed with brine, dried over Na2S04, filtered, and concentrated in vacuo. Flash column chromatography (silica gel, 0-3.5 % MeOH in CH2C12) afforded the title compound as a colorless thin film (116 mg). MS (ESI, pos. ion) m/z: 364 (M+H).
Example 154-2-((25)-BicycIo [2.2.1] h eptan-2-ylamin o)-5-methyl-5-((l -(methylsulfonyl)piperidin-4-yl)methyI)thiazoI-4(5-H)-one. 128
[0804] To a solution of 2-((2 ')-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-( iperidin-4-ylmethyl)thiazol-4(5H)-one (64 mg, 0.20 mmol) in CH2C12 (1.5 mL) was added nlethanesulfonyl chloride (Aldrich, 34 mg, 0.30 mmol) and triethylamine (60 mg, 0.60 mmol), and the reaction mixture was stirred at room temperature for ca. 18 h. Water (30 mL) was then added, and the crude product was extracted with CH2C12 (3 x 60 mL). The combined organic extracts were washed with brine, dried over Na2S04, filtered, and concentrated in vacuo. Flash column chromatography (silica gel, 0-3 % MeOH in CH2C12) afforded the title compound as a white solid (34 mg). MS (ESI, pos. ion) m/z: 400 (M+H).
Example 155-2-((15 25,,4i?)-Bicyclo[2.2.1]heptaii-2-ylamino)-5-(2-brornoethyl)thiazoI-4(5H)-one METHOD NN
[0805] To a solution of 2-((l-?,25,4i?)-bicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one (2.98 g, 14.2 mmol) in THF (15 ml) at -78 °C was added LDA (2.0 N, 28.4 ml). After 5 min, 1,2-dibromoethane (4.87 mL, 56.8 mmol) was added, and the reaction mixture was stirred for 3 h at -78°C. The resulting reaction mixture was poured into sat'd NaH2P04 and extracted with EtOAc. The organic layer was dried over MgS04, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as a white solid. MS (ES+): 317 (M+H)+.
Example 156-2-((liS 2S,4i?)-Bicyclo[2.2.1]hept-2-ylamino)-6,6-dimethyl-7-oxa-l-thia-3-azaspiro[4.4]non-2-en-4-one and 5-((lS',25,,4 ?)-bicyclo[2.2.1]hept-2-yIamino)-4-thia-6-azaspiro [2.4] h ept-5-en-7-one. 129
[0806] To a solution of 2-((llS,,2. ,4i?)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-bromoethyl)thiazol-4(5H)-one (134 mg, 0.5 mmol) in THF (1 mL) at -78 °C was added LDA (2.0 N, 1.25 ml). After 5 min, acetone (500 uL) was added, and the reaction mixture was stirred for 3 h at -78°C. The resulting reaction mixture was poured into a sat'd NaH2P04 and extracted with EtOAc. The organic layer was dried over MgS04, filtered and concentrated in vacuo. The crude residue was purified through flash chromatography (4:1 ; Hexane:EtOAc) to give 2-((lS,25,4i?)-bicyclo[2.2.1]hept-2-ylamino)-6,6-dimethyl-7-oxa-l-thia-3-azaspiro[4.4]non-2-en-4-one as a white solid. (MS (ES+): 295 (M+H)+), and 5-((l£,2,S,4R)-bicyclo[2.2.1]hept-2-ylamino)-4-thia-6-azaspiro[2.4]hept-5-en-7-one as a white solid. MS (ES+): 237 (M+H)+.
Example 157-2-(2-(Bicyclo[2.2.1]heptan-2-yIamino)-4-oxo-4,5-dihydrothiazol-5-yl)acetic acid METHOD OO
[0807] A stirred mixture of (±)-exo-l -(bicyck>r2.2.1 lheptan-2-yl)thiourea (1.00 e„ 5.87 mmol) and maleic anhydride (576 mg, 5.87 mmol) in glacial acetic acid (20 mL) was heated to reflux. After 1 h, the solvent was evaporated in vacuo, and the residue was azeotroped from toluene (3 x 15 mL). The resulting solid was suspended in water, filtered, washed with water (3 x 15 mL) and then hexane (2 x 10 mL). Air drying the solid afforded the title compound (1.57 g) as a cream-colored amorphous solid. 130 Example 158-5-(2-(Azepan-l-yl)-2-oxoethyl)-(±)-exo-2-(bicycIo[2.2.1)heptan-2-ylamino)thiazoI-4(5H)-one
[0808] To a stirred solution of 2-(2-(bicyclo[2.2.1]heptan-2-ylamino)-4-oxo-4,5-dihydrothiazol-5-yl)acetic acid (518 mg, 1.93 mmol) in N,N-dimethylformamide (20 mL) were added N,N-diisopropylethylamine (0.404 mL, 2.32 mmol) and 0-(7-azabenzotriazol-l-yl)-N,N,N\N-tetramethyluromum hexafluorophosphate (807 mg, 2.12 mmol) at room temperature. After 20 min, hexamethyleneimine (0.218 mL, 1.93 mmol) was added. After an additional 3 h, the reaction was diluted with ethyl acetate (40 mL), washed with water (25 mL), and then brine (30 mL). The organic layer was then dried over sodium sulfate, filtered,-and concentrated in vacuo. The residue was purified by flash chromatography (Si02, dichloromethane/methanol, 98:2 to 97:3) to afford the title compound (472 mg) as a cream-colored amorphous solid. MS (ESI, pos. ion) m/z: 350.2 (M+H).
Example 159-2-(2-(Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yI)ethyl isonicotinate METHOD PP
[0809] A mixture of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxyethyl)-5-methylthiazol-4(5H)-one (0.080 g, 0.30 mmol), isonicotinoyl chloride hydrochloride (0.056, 0.30 mmol), and N,N-diisopropylethylamine (0.13 mL, 0.75 mmol) in C¾C12( 1.0 mL) was heated in a sealed tube in a microwave oven (SmithSynthesizer from Personal Chemistry) at 120 °C for 10 min. The reaction mixture was cone, in vacuo, and the residue was partitioned 131 between EtOAc and water. The organic portion was separated, washed with brine, cone, in vacuo, and purified by RP-HPLC to give the title compound as a white solid. MS m/z: 374.1 (M+H)+.
Example 160-2-((25)-Bicyclo[2.2.1]heptan-2-yIamino)-5-methyl-5-((l-(3-(2-morpholinoethoxy)benzoyl)piperidin-4-yl)methyl)thiazol-4(5H)-one.
[0810] (a) 4.0-4.7 M HCl/EtOAc, room temperature; (b) RCOOH, EDCI, HOBt or (RCO)A (Et)3N; (c) (C1CH2C¾)20, KI, 2C03 -((l-(3 2-Aminoethoxy)benzoyl)piper^ ylamino)-5-methylthiazol-4(5i?)-one. 132
[0811] The title compound was prepared according to the procedure described in the preparation of 2-((25)-bicyclo[2.2.1]heptari-2-ylarnino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one by using terf-butyl 2-(3-(4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine- 1 -carbonyl)phenoxy)ethylcarbamate (689 mg, 1.18 mmol) as the starting material. The title compound was obtained as an off-white solid (531 mg). MS (ESI, pos. ion) m/z: 485 (M+H) A^-(2-(3-(4-((2-((25)-Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yI)meth l)piperidine-l-carbonyl)phenoxy)ethyI)furan-3-carboxamide.
[0813] The title compound was prepared according to the procedure described in the preparation of tert-butyl 2-(3-(4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-l-carbonyI)phenoxy)ethylcarbamate by using 5-((1 -(3-(2-aminoethoxy)benzoyl)piperidin-4-yl)methyl)-2-((21S)-bicyclo[2.2.1 ]heptan-2-ylamino)-5-methylthiazol-4(5H)-one (93 mg, 0.19 mmol), 3-furoic acid (Aldrich, 39 mg, 0.35 mmol), EDCI (Aldrich, 74 mg, 0.38 mmol), HOBt (Aldrich, 5.2 mg, 0.038 mmol) and triethylamine (Aldrich, 39 mg, 0.38 mmol, 2.0 eq). The title compound was obtained as an off-white solid (89 mg). MS (ESI, pos. ion) m/z. 579 (M+H). 2-((25)-Bicyclo[2.2.1iheptan-2-ylamino)-5-methyl-5-((l-(3-(2-morpholinoethoxy)benzoyl)piperidin-4-yl)methyl)thiazol-4(5H)-one. 133
[0815] A mixture of 5-((l-(3-(2-aminoethoxy)benzoyl)piperidin-4-yl)methyl)-2- ((25)-bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one (100 mg, 0.207 mmol), . K2C03 (114 mg, 0.83 mmol), KI (Aldrich, 6.9 mg, 0.041 mmol), l-chloro-2-(2- chloroethoxy)ethane (Aldrich, 38 mg, 0.27 mmol) in CH2C12 (3 mL) was heated at reflux for 10 d. Saturated NaHC03 (50 mL) was added, and the crude product was extracted with CH2C12 (4 x 60 mL). The combined organic layers were washed with brine, dried over Na2S04, filtered, and concentrated in vacuo. Flash column chromatography (silica gel, CH2C12 with 0-4% MeOH) afforded the title compound as a colorless thin film (10 mg). MS (ESI, pos. ion) m/z: 555 (M+H).
[0816] The following table of compounds were prepared using the methodologies outlined above.
TABLE 1 134 136 137 138 139 140 141 142 143 144 145 2 146 147 Mol Mass Methods of Structure Name Wt. Spec Prep. 2-((S)-l-(4- 0 252.3 253 fluorophenyl)ethylamino)-5- X methylthiazol-4(5H)^one (R)-2-((lS,2S,4R)- iv. H H bicyclo[2.2.1]heptan-2- 0 292.3 293 ylamino)-5-methyl-5- Y H 7 "CF3 (trifluoromethyl)thiazol-4(5H)- CC one (S)-2-((lS,2S,4R)- k H H bicyclo[2.2.1]heptan-2- 0 292.3 293 ylamino)-5-methyl-5- Y H CF3 (trifluoromethyl)thiazol-4(5H)- CC one 0 5-isopropyl-5-methyl-2-((R)-l - (2- z 344.4 345 (trifluoromethyl)phenyl)ethyla AA 148 149 150 151 152 153 154 156 157 158 159 160 161 162 163 164 165 166 167 168 169 Mol Mass Methods of Structure Name Wt. Spec Prep.
P 2-(cyclohexylamino)-5-ethyl-5- 240.4 241 L methylthiazol-4(5H)-one .
H X 2-bicyclo[2.2. l]heptan-2- L 252.4 253 ylamino)-5-ethyl-5- X methylthiazol-4(5H)-one -ethyl-5-methyl-2- P 292.4 293 (tricyclo[3.3.1.1~3,7~]dec-l- L \ ylamino)- 1 ,3 -thiazol-4(5H)-one X 0 2-(cyclohexylmethylamino)-5- P 254.4 255 ethyl-5-methylthiazol-4(5H)- L one X 2-((lS,2S,4R)- L bicyclo[2.2. l]hept-2-ylamino)- 264.4 265 X H l-thia-3-azaspiro[4.4]non-2-en- 170 171 172 173 1 s 292.4 293 (tricyclo[3.3.1.0~3,7~]non-3- L ylamino)-l,3-thiazol-4(5H)-one X 2-(bicyclo[2.2. l]heptan-2- X 436/43 ylamino)-5-(2-((3- 436.4 JJ 8 bromophenyl)(met yl)amino)et hyl)-5-methylthiazo]-4(5H)-one Br (3i?)-ethyl 3-(2-(2- (bicyclo[2.2.1]heptan-2- X 435.5 436 ylamino)-5-methyl-4-oxo-4,5- JJ i 0 dihydrothiazol-5- F F yl)ethylamino)-4,4,4- 174 175 Mol Mass Methods of Structure Name Wt. Spec Prep. 8-(methyloxy)-2- O (tricyclo[3.3.1.0~3,7~]non-3- 334.5 335 L . ylamino)-l -thia-3 - X azaspiro[4.5]dec-2-en-4-one 2-((cyclohexylmethyl)amino)- P 310.5 311 8-(methyloxy)- 1 -thia-3- L azaspiro[4.5]dec-2-en-4-one X 2-(cyclohexylamino)-8- P 296.4 297 (methyloxy)- 1 -thia-3- L 0 azaspiro[4.5]dec-2-en-4-one X ' 1 2-(cycloheptylamino)-8- P 310.5 311 (methyloxy)- 1 -thia-3 - L 0 azaspiro[4.5]dec-2-en-4-one X 1 L 304.4 305 methylphenyl)amino)- 1 -thia-3- X azaspiro[4.5]dec-2-en-4-one 2-(cyclohexylamino)-7- P 296.4 297 (methyloxy)- 1 -thia-3 - L azaspiro[4.5]dec-2-en-4-one X 2-((cyclohexylmethyl)amino)- P 310.5 311 7-(methyloxy)- 1 -thia-3- L azaspiro[4.5]dec-2-en-4-one X 2-(cycloheptylamino)-7- P >° 310.5 311 (methyloxy)- 1 -thia-3 - L azaspiro[4.5]dec-2-en-4-one X 176 Mol Mass Methods of Structure Name Wt. Spec Prep. 2-(cyclooctylamino)-7- O s r° 324.5 325 (methyloxy)- 1 -thia-3- L azaspiro[4.5]dec-2-en-4-one X 2-(bicyelo[2.2.1]hept-2- ylamino)-5-methyl-5-(2-((6- X 374.5 375 (methyloxy)-3- JJ pyridinyl)amino)ethyI)- 1 ,3- thiazol-4(5H)-one 2-(bicyclo[2.2.1]hept-2- X ylamino)-5-(2-(4- 394.5 395 JJ isoquinolinylarnino)ethyl)-5 - methyl-1 ,3-thiazol-4(5H)-one 2-bicyclo[2.2.1]hept-2- L H 308.4 309 ylamino)-7-(methyloxy)- 1 -thia- X 3-azaspiro[4.5]dec-2-en-4-one 2'-((lS,2S,4R)- bicyclo[2.2 l]heptan-2-ylamino- N 346.4 . 347 6-fluoro-2,3-dihydro-spiro[4H- X H FjQr° 1 -benzopyran-4,5 ' (4Ή)- thiazo]-4'-one 2'-((lS,2S,4R bicyclo[2.21]heptan-2-ylamino- N 363/36 362.9 6-chloro-2,3-dihydro-spiro[4H- X H 5 l-benzopyran-4,5 '(4'H)- thiazo]-4'-one 177 178 179 180 181 182 183 184 185 186 187 188 Mol Mass Methods of Structure Name Wt. Spec Prep. 2-(bicyclo[2.2.1]heptan-l- 224.3 225 ylamino)-5-methylthiazol- Y 4(5H)-one tert-butyl 4-((2- (bicyclo [2.2.1 Jheptan- 1 - ylamino)-5-methyl-4-oxo-4,5- Y 421.6 422 dihydrothiazol-5- LL yl)methyl)piperidine- 1 - carboxylate 2-(bicyclo [2.2.1 Jheptan- 1 - Y ylamino)-5-memyl-5- 321.5 322 LL (piperidin-4-ylmethyl)thiazol- MM(a) 4(5H)-one 2-(bicyclo [2.2.1 ]heptan- 1 - ylamino)-5 -(( 1 -(furan-3 - Y " 415.6 416 carbonyl)piperidin-4- LL yl)methyl)-5-methylthiazol- MM 4(5H)-one -((l-acetylpiperidin-4- yl)methyl)-2- Y 363.5 364 (bicyclo[2.2.1]heptan-l- LL ylamino)-5-methylthiazol- MM 4(5H)-one 189 190 191 192 Mol Mass Methods of Structure Name wt. ■ Spec Prep. thiazole-5-carboxylate -(l-methylethyl)-2- 292.4 293 (tricyclo[3.3.1.1~3,7~]dec-l- X ylamino)- 1 ,3-thiazol-4(5H)-one -phenyl-2- 326.5 327 (tricyclo[3.3.1.1 ~3 ,7~]dec- 1 - X ylamino)- 1 ,3-thiazol-4(5H)-one -(l-met ylethyl)-5- (methyloxy)-2- 322.5 323 II . (tricyclo[3.3.1.1~3,7~]dec-l- ylammo)-l,3-thiazol-4(5H)-one -methyl-2- 264.4 265 (tricyclo[3.3.1.1~3,7~]dec-l- X ylamino)-l,3-thiazol-4(5H)-one -(l-methylethyl)-2-(3- 235.3 236 pyridinylamino)- 1 ,3-thiazol- X 4(5H)-one 2-((4-cyclohexylphenyl)amino)- 316.5 317 5-( 1 -methylethyl)- 1 ,3 -thiazol- X 4(5H)-one xp 5 -methyl- 5 -phenyl-2- 340.5 341 (tricyclo[3.3.1.1~3,7~]dec-l- X ylamino)-l,3-thiazol-4(5H)-one -(l-methylethyl)-2-((2- 264.3 265 (methyloxy)phenyl)amino)- 1,3- . X thiazol-4(5H)-one 193 Mol Mass Methods of Structure Name Wt. Spec Prep. -methyl-5-(l -pyrrolidinyl)-2- 333.5 334 (tricyclo[3.3.1. l~3,7~]dec- 1 - II ylamiiio)- 1 ,3 -thiazol-4(5H)-one 0 y 5-(methylamino)-5-(l - A NH methylethyl)-2- 321.5 322 II (tricyclo[3.3.1.1 ~3,7~]dec- 1 - ylamino)-l ,3-thiazol-4(5H)-one -(l-methylethyl)-2-(2- 235.3 236 pyridinylamino)-l,3-thiazol- X 4(5H)-one 2-((4-fluorophenyl)amino)-5- 252.3 253 (l-methylethyl)-l,3-thiazol- X 4(5H)-one H 5-(l-methylet yl)-2-(4- 235.3 236 pyridinylamino)- 1 ,3 -thiazol- X / ■v--1^ 2-((2,4-difluorophenyl)amino)- 270.3 271 5-(l -methylethyl)-l ,3-thiazol- X 4(5H)-one -(l-methylethyl)-2-((2- 248.4 249 methylphenyl)amino)-l ,3- X thiazol-4(5H)-one -methyl-5-(methyloxy)-2- X 294.4 295 (tricyclo[3.3.1. l~3,7~]dec-l - II ylamino)-! ,3-thiazol-4(5H)-one 194 195 2 5 1 1 196 197 268.3 269 (2-hydroxyethyl)-5-methyl- 1 ,3- KK thiazol-4(5H)-one -(l -methylethyl)-2-(((2R)- tetrahydro-2- 242.3 243 X furanylmethyl)amino)- 1,3- thiazol-4(5H)-one -(l-methylethyl)-2-((3- 264.4 265 (methyloxy)phenyl)amino)-l ,3- X thiazol-4(5H)-one 198 199 Mol Mass Methods of Structure Name Wt. Spec Prep. -(l-methylethyl)-2-((2-methyl- 278.4 279 3-(methyloxy)phenyl)amino)- X l,3-thiazol-4(5H)-one 2-((2,6-dichlorophenyl)amino)- 303.2 304 5-(l-methylethyl)-l,3-thiazol- X 4(5H)-one 2-((2-chlorophenyl)amino)-5- 298.8 299 methyl-5-(2-(methyloxy)ethyl)- AA l,3-thiazol-4(5H)-one \ 2-((2-chlorophenyl)amino)-5- 284.8 285 methyl-5-((methyloxy)methyl)- AA ά h l,3-thiazol-4(5H)-one 2-((3-chloro-2- methylphenyl)amino)-5-niethyl- 200 201 Mol Mass Methods of Structure Name Wt. Spec Prep. 2-((lS,2S,4R)- bicyclo[2.2. l]hept-2-ylaniino)- 280.4 281 EE H 8-oxa-l-thia-3- azaspiro[4.5]dec-2-en-4-one 2-((lS,2S,4R)- bicyclo[2.2.1 ]hept-2-ylamino)- H 294.4 295 EE 7-(methyloxy)-l-thia-3- 1 azaspiro[4.4]non-2-en-4-one 2-((2-chlorophenyl)amino)-7- 310.8 311 (methyloxy)- 1 -thia-3- EE azaspiro[4.4]non-2-en-4-one 2-((2 -methyl- 1 ,3-benzothiazol- 305.4 306 5-yl)amino)-5-(l-methylethyl)- X l,3-thiazol-4(5H)-one 202 203 204 206 Mol Mass Methods of Structure Name Wt. Spec Prep. [4.5] dec-2-en-4-one X
[0817] The following compounds are encompassed by the present invention and are prepared by one of the methodologies described herein: 207 208 209 210 211 212 213 214 215 216 217 218 GENERAL METHODOLOGIES QQ-YY METHOD QQ
[0819] leq. of 3-bromopyrrolidin-2-one (J. Med. Chem. 1987, 30, 1995-1998. H. D uta, H. Shirota, S. Kobayashi, Y. Yamagashi, K. Yamada, I. Yamatsu, K. Katayama) and 1.0 eq. of the appropriate thiourea were dissolved in acetone and heated to reflux for 8h. The reaction mixture was cooled to RT, NaHC03 (sat. solution) was added and the aqueous phase extracted with DCM. The organic phase was separated and concentrated in vacuo to give the crude product. The obtained crude product was dissolved in pyridine and a few drops of DMF were added followed by the appropriate benzoyl chloride (3.0 eq.) and the reaction mixture was shaken at RT. 10% HC1 was added and the mixture extracted with DCM. The organic phase was concentrated in vaccum. Purification was performed using preparative HPLC.
Example 161-N-{2-[2-(bicycIo[2.2J]hept-5-en-2-ylamino)-4-oxo-4,5-dihydro-1 -thiazoI-5-yl]ethyl}-6-chloronicotinamide
[0820] 5-(2-aminoethyl)-2-(bicyclo[2.2.1 ]hept-5-en-2-ylamino)- 1 ,3-thiazol-4(5H)-one (0.050 g, 0.199 mmol) was suspended in MeCN (1 ml). 6-chloronicotinoyl chloride (O.140 g, 0.796 rnmol) dissolved in MeCN (1 ml) was added and the reaction mixture was shaken at room temperature for 18 h. Solvents were removed in vacuo. Purification was erformed using preparative HPLC (System A, 20-40% MeCN over 5 min). 108211 1H NMR (500 MHz, Solvent) 1.44-1.79 (m, 5 H) 2.12-2.28 (m, 1 H) 2.40-2.49 (m, 1 H) 2.84-3.02 (m, 2 H) 3.56-3.65 (m, 2 H) 3.76 (d, J=7.54 Hz, 1 H) 4.37-4.47 (m, 1 H) 6.02-6.11 (m, 1 H) 6.19-6.24 (m, 1 H) 7.52-7.56 (m, 1 H) 8.15-8.20 (m, 1 H). 219
[0822] HPLC-MS: 93 %, RT = 1.74 min (System A, 10-97% MeCN over 3 min), 92 %, RT = 1.60 min (System B, 10-97% MeCN over 3 min)
[0823] MS (ESI+) for C18H19N4O2S m/z 391 (M+H)+ METHOD RR
[0824] 1.0 cq. of the appropriate thiourea and maleic anhydride (1.0 eq.) were heated to reflux in acetone for 5 h, yielding a white emulsion. Evaporation in vacuo afforded a white solid. The product was triturated with DCM, collected on a filter and air-dried giving the carboxylic acid product as a white powder.
[0825] The carboxylic acid (1.0 eq). and 2-chloro-l-methylpyridinium iodide (1.2 eq.), or similar coupling agent, were mixed in DCM for 10 minutes before the amine (1.0 eq.) was added followed by Et3N (1.5 eq.). The reaction mixture was stirred at RT for 16 h. The reaction mixture was poured onto a Hydromatrix column (pretreated with 1 M HCl) and the crude product was eluted with DCM. The obtained crude product was purified by reverse phase.
Example 162-2-{2-[(cycIohexylmethyl)amino]-4-oxo-4,5-dihydro-l,3-thiazol-5-yl}-N-(cyclopropylmethyl)-N-propylacetamide
[0826] Cyclohexylmethyl thiourea (0,85g, 4,94mmol) and maleic anhydride (4.8g, 4.94mmol) were refluxed over night at 110°C in acetic acid. The reaction was concentrated and triturated with EtOAc to give the product as a pure off-white solid. MS m/z 271 (M+H)+ 220 To a suspension of {2-[(cyclohexylmethyl)amino]-4-oxo-4,5-dihydro-l,3-thiazol-5-yl}acetic acid in DCM 5ml was added thionyl chloride 1.5eq and the reaction stirred for 30 minutes. The secondary amine (3eq) was added and the reaction stirred overnight. Concentration and purification by reverse phase chromatography yielded the desired product. • 108271 Ή NMR (400 MHz, CHLOROFORM-D) δ ppm 0.26 (m, J=3.8, 1.10 Hz, 2 H) 0.54 (m, J=S.l, 1.22 Hz, 1 H) 0.65 (m, J=7.3 Hz, 1 H) 0.93 (m, 6 H) 1.25 (m, 3 H) 1.71 (m, 8 H) 2.82 (m, J=12.2 Hz, 1 H) 3.11 (m, 1 H) 3.23 (m, J=6.5 Hz, 2 H) 3.29 (m, 2 H) 3.42 (m, 1 H) 3.54 (m, 1 H) 4.44 (m, J=10.4, 1.7 Hz, 1 H) MS m/z 366 (M+H)+
[0828] HPLC 100% RT=3,15 min (System A. 10-97% MeCN over 3 min), 100% (System B. 2-95% MeCN over 2 min).
Method SS
[0829] The synthesis of oxazolone analogues was carried out using the procedure detailed in the scheme below.
[0830] The oxazolones (F) were prepared according to the reaction scheme above from commercially available ketones (A), a-hydroxy acids (C), or ct-hydroxy esters (D).
[0831] i) To a mixture of ketone (A) (1 eq) and KCN (1.1 eq) in H20 at 0 °C was added 40% H2S04 over 40 min. After stirring the reaction for an additional 1 h at ambient temperature, diethyl ether and H20 were added. The phases were separated, and the aqueous layer was extracted with diethyl ether. The combined organic phases were washed with brine, dried over MgS04, and concentrated in vacuo to yield cyanohydrine (B).
[0832] ii) The cyanohydrine (B) was dissolved in concentrated HC1 and the mixture was stirred under heating for 8—48 h. The solvent was evaporated, and the residue was dried Z7z vacuo to give the crude acid (C).
[0833] iii) To a solution of the a-hydroxy acid (C) in ethanol was added acid catalyst, and the mixture was stirred under reflux for 1-3 days. The solvent was removed to give α-hydroxy ester (D). 221
[0834] iv) A mixture of oc-hydroxy ester (D) (1 eq) and guanidine (1-3 eq) in ethanol was stirred under reflux overnight. The solvent was removed, and the residue was purified by recrystalization from water/ethyl acetate (alternatively silica gel flash chromatography) to give 2-aminooxazolone (E).
[0835] v) A mixture of 2-aminooxazolone (E) (1 eq) and amine (2.5-3 eq) in 99.5% ethanol was heated in microwave oven for 20—120 in at 160—180 °C. The solvent was removed, and the residue was purified by reverse-phase preparative HPLC to give oxazolone (F).
[0836] Spiropiperidines (H) were obtained from F' (synthesized from the corresponding ketone A) according to the scheme above.
[0837] vi) To a solution of the benzyl protected intermediate (F') in 2-methoxyethanol was added catalytic amounts of 5% Pd/C and the mixture was exposed to H2 (50-60 psi) for 5-24 h. Celite was added to the reaction mixture, and after filtration and removal of the solvent crude spiropiperidine G was obtained.
[0838] vii) To a solution of spiropiperidine G (1 eq) and aldehyde (1 eq) in dichloroethane was added sodium triacetoxyborohydride (1.4 eq) and the reaction mixture was stirred at _ - >υ u ovemignt. i e material was punned by reverse-phase preparative HPLC to give the product H.
Examples 163- 2-Hydroxy-2,3-dimethylbutanenitriIe
[0839] To mixture of 3-methylbutan-2-one (4.71 g, 54.7 mmol) and CN (3.92 g, 60.2 mmol) in H20 (10 mL) was dropwise added 40% H2S04 (10 mL) over 40 min. The temperature was raised to ambient, and after stirring the reaction for 1 h,. diethyl ether (25 mL) and ¾0 (15 mL) were added. The aqueous layer was extracted with diethyl ether (25 mL), and the combined organic phases were washed with brine (10 mL) and dried over MgS0 . Evaporation of the solvent yielded the product as a colorless liquid. 222 Example 164-2-Hydroxy-2,3-dimethyIbutanoic acid
[0840] A solution of 2-hydroxy-2,3-dimethylbutanenitrile (4.71 g, 54.7 mmol) in concentrated HCI was stirred at 75 °C for 5 h and then under reflux for 8 h. The solvent was removed to give the crude title compound as an off-white solid.
Example 165-Ethyl 2-hydroxy-2,3-dimethylbutanoate EtO
[0841] To a solution of 2-hydroxy-2,3-dimethylbutanoic acid (5.53 g, 41.8 mmol) in 99.5% ethanol (200 mL) was added 2 M HCI in diethyl ether (8 mL) and the mixture was stirred under reflux for 3 days. The solvent was carefully removed to give the crude a-hydroxy ester as a pale yellow liquid.
Example 166-2- Amino- 5-isopropyI-5-methyI-l,3-oxazoI-4(5H)-one
[0842] A mixture of ethyl 2-hydroxy-2,3-dimethylbutanoate (2.92 g, 1S.2 mmol), guanidine hydrochloride (1.74 g, 18.2 mmol), and K2C03 (2.52 g, 18.2 mmol) in 99.5% ethanol (40 mL) was stirred under reflux for 20 h. The solvent was removed, and the residue was purified by silica gel flash chromatography (ethyl acetate/methanol 9: 1) to give the product as a white solid.
Example 167-2-(Cyclooctylamino)-5-isopropyl-5-methyl-l,3-oxazol-4(5j¾ -dne
[0843] A solution of 2-amino-5-isopropyl-5-methyl-l,3-oxazol-4(5H)-one (55.7 mg, 0.357 mmol) and cyclooctylamine (147 μΐ, 1.07 mmol) in 99.5% ethanol (1 mL) was heated 223 in microwave oven in a sealed tube for 40 min at 180 °C. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC chromatography to yield the product as a white solid.
[0844] HPLC 100%, RT = 2.56 (System A, 10-97% MeCN over 3 min), 100%, RT = 1.47 min (System B, 2-95% MeCN over 2 min). 108451 Ή NMR (400 MHz, DMSO-J6) δ 0.77-0.79 (m, 3 H), 0.90-0.93 (m, 3 H), 1.29 (s, 2.1 H, major rotamer), 1.31 (s, 0.9 H, minor rotamer), 1.40-1.80 (m, 14 H), 1.84-1.94 (m, 1 H), 3.67-3.77 (m, 1 H), 8.67 (d, J= 7.9 Hz, 0.7 H, major isomer), 8.95 (d, J= 7.9 Hz, 0.3 H, minor isomer).
[0846] MS (ESI+) for Ci5H26N202 m/z 267 (M+H)+.
METHOD TT
[0847] W
[0848] R and R' are bivalent alkylene and form a 3-8 membered ring with the nitrogen to which they are attached.
[0849] The thiazalones K were prepared according to the reaction scheme above from commercially available hydrazines. To a mixture of hydrazine 1 (1 eq) in DCM (5 mL/mmol amine) was added ethoxycarbonyhsocyanate (1.1 eq) and the mixture stirred for lh at ambient temperature, followed by addition of 5M aq NaOH (5 mL/mmol amine) and heating for l-2h at 65°C. The cooled solution was extracted twice with DCM, then the combined organic layers washed consecutively with saturated aq NaHC03, water and brine, and finally concentrated to give the thiourea J. Thiourea J (1 eq) was reacted with the appropriate a-bromoester (1 eq) in the presence of diisopropylethylamine (1.1 eq) in EtOH (5 mL/mmol) in the microwave oven for l-2h 150-155°C, or by thermal heating at 95-140°C for 224 several days in dioxane (1 mL/mmol) in the absence of base. Concentration followed by chromatographic purification gave the thiazalone K; Example 168-2-(Azepan-l-ylamino)-5-isopropyl-l,3-thiazol-4(5H)-one
[0850] N-(Homopiperidine)thiourea was prepared by stirring a mixture of aminopiperidine ( 1 .0 g, 8.8 mmol) and ethoxycarbonylisocyanate (1.1 mL, 9.7 mmol) in DCM (50 mL) for 1 h, followed by addition of 5M aq NaOH (50 mL) and heating for 2h at 65°C, during which time DCM evaporates. The cooled solution was extracted twice with DCM, then the combined organic layers washed consecutively with saturated aq NaHC03, water and brine, and finally concentrated.
[0851] This thiourea (150 mg, 0.87 mmol) was then reacted with ethyl 2-bromoisovalerate (150μί, 0.87 mmol) in the presence of Hunigs base (diisopropylethylamine, 160/iL, 0.96 mmol) in EtOH (4 mL) in the microwave for lh 15 min at 150°C. Concentration followed by purification by reversed-phase HPLC, then made basic with aq NaHC03, gave the product as a white solid. Ή NMR (400 MHz, DMSO-D6) δ ppm 0.74 (d, J=6.59 Hz, 3 H) 0.91 (d, J=6.84 Hz, 3 H) 1.52 (d, J=2.20 Hz, 4 H) 1.60 (s, 4 H) 2.26 (td, J=6.53, 4.03 Hz, 1 H) 2.80 - 2.86 (m, 4 H) 3.95 - 4.00 (m, 1 H). MS(ESI) for Ci2H2iN3OS m/z 256 (M+H).
METHOD UU
[0852] R'2 = alkyl or aryl, R = cycloalkyl, X = O or N, Y = C, O or N
[0853] The thiazalones were prepared according to the reaction scheme above from L (L was prepared according to Method A), (iii) To a solution of L (leq) in CC14 (12 mL/mmol L) was added N-bromosuccinimide (1.5 eq) and warmed to 60-70°C for lh. The 225 warm mixture was filtered and the filtrate concentrated to give the bromo intermediate M. (iv) Reaction of M with an alcohol (10-40 eq in THF or neat) at ambient temp - 70°C for 2-24h gave, after concentration and purification, the ethers N (X=0 Y=C,0). Reaction of M with a chloroalcohol (20 eq in THF) at 60°C for 3-24h gave, after concentration and purification, the chloroether intermediates. Amination was performed by warming a solution of the chloroether (1 eq) in THF (0.3 mL/mmol chloroether) with an amine (0.3 mL/mmol chloroether) and a crystal of Nal either thermally at 80°C for 4-24h or in the microwave oven 180°C lh. Concentration and purification gave the aminoethers N (X=0 Y=N). Reaction of M with an amine (10-40 eq in THF or neat) at ambient temp for 10-30 min gave, after concentration and purification, the amines N (X=N Y=C,N).
Example 169-2-(Bicyclo[2.2.1]hept-2-yIamino)-5-methyI-5-(3-morpholin-4-yIpropoxy)-1 ,3-thiazol-4(5H)-one
[0854] To a solution of the thiazolone (150 mg, 0.67 mmol) in CC (5 mL), was added N-bromosuccinimide (143 mg, 0.80 mmol) and warmed to 60°C. After lh, the mixture was filtered warm and concentrated to yield 244 mg of the product as a yellow solid. THF (3 mL) and 3-chloropropanol (2.2 niL, 26.8 mmol) were added and the solution warmed to 60°C overnight. The resulting solution was concentrated and the product was purified by reversed-phase HPLC, then made basic with aq NaHCC*3, to yield the chloroether as a colourless oil.
[0855] Morpholine (3 mL) and THF (3 mL) were added and the solution was allowed to stir at 80°C for 4h. The resulting solution was concentrated and the product was purified by reversed-phase HPLC, then made basic with aq NaHC03, to yield the product as a white solid. Ή NMR (400 MHz, DMSO-D6) δ ppm 1.06 - 1.18 (m, 3 H) 1.36 - 1.48 (m, 4 H) 1.58 - 1.64 (m, 2 H) 1.66 - 1.71 (m, 3 H) 2.19 - 2.30 (m, 8 H) 3.09 - 3.17 (m, 2 H) 3.37 - 3.45 (m, 1 H) 3.48 - 3.57 (m, 4 H), 3.80 (m, 0.5H) 4.05 (m, 0.5H). MS(ESI) for C,8H29N303S m/z 368 (M+H). 226 Example 170-2-(Bicyclo[2.2.1]hept-2-ylamino)-6-0xa-l-thia-3-azaspiro[4.4]non-2-en-4-one
[0856] To a continuously N2-flushed solution of the thiazolone (200 mg, 0.95 mmol) in dry THF (10 mL) was added lithium diisopropylamide (1.9 mL of a 2M solution in THF/heptane/ethyl benzene, 3.8 mmol) at -78°C. The resulting brown solution was allowed to stir lh at this temperature after which time (3-bromopropoxy)te/-t-butyldimethylsilane (0.6 mL, 2.6 mmol) was added and the solution allowed to warm to 5°C (2.5h). The reaction was quenched with 6 mL 2/1 MeOH/HOAc followed by addition of a saturated solution of aq NaHC03. The silyl-protected product (50% conversion according to HPLC) was extracted with EtOAc and the resulting solution was concentrated and the product was purified by reversed-phase HPLC. During purification, the alcohol function was deprotected to give the free alcohol.
[0857] To the free alcohol (0.17 mmol) in DCM (5 mL) was added Br2 (ΙΟμΙ,, 0.17 mmol) and a drop HBr (48% aqueous) and warmed to 60°C lh. The resulting solution was quenched with aq NaS20 and extracted with DCM. The product was purified by reversed-phase HPLC, then made basic with aq NaHC03, to yield the product as a white solid. Ή NMR (400 MHz, CHLOROFORM-D) δ ppm 1.09 - 1.19 (m, 2 H) 1.21 - 1.30 (m, 2 H) 1.49 -1.59 (m, 2 H) 1.70 - 1.77 (m, 1 H) 1.93 (d, J=2.93 Hz, 1 H) 1.99 - 2.10 (m, 1 H) 2.22 - 2.32 (m, 1 H) 2.36 - 2.48 (m, 3 H) 2.66 (dt, J=9.22, 4.55 Hz, 1 H) 3.30 - 3.36 (m, 1 H) 4.04 - 4.14 (m, 1 H) 4.15 - 4.23 (m, 1 H). MS(ESI) for C13H,8N202S m/z 267 (M+H).
METHOD W
[0858] The following examples serve to illustrate the preparative procedure employed for the synthesis of thiazolone analogues containing a heterocyclic side-chain at the 5-position. 227 Example 171-N-(2-Aminophenyl)-2-(2-anilino-4-oxo-4,5-dihydro-l,3-thiazoI-5-yl)acetamide
[0859] N-(2-Aminophenyl)-2-(2-anilino-4-oxo-4,5-dihydro- 1 ,3-thiazol-5-yl)acetic acid, prepared using method 2 above, (30 mg, 1 eq) was dissolved in a mixture of DCM/DMF (2 mL/2 mL) and O-phenylendiamine (15 mg, 1.1 eq), and l-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDC, 30 mg, 1.3 eq) were then added sequentially. The reaction mixture was stirred 40 °C for 2 h. Separated between DCM and H20, the organic layer concentrated to give a crude orange brown oil used directly in the next step: HPLC 43%, RT= 0.93 min (System B, 2-95% MeCN over 2 min); MS [M+H]+ m/z = 34 .
Example 172-2-Anilino-5-(l^f-benzimidazol-2-ylmethyl)-l,3-thiazoI-4(5H)-one
[0860] N-(2-Aminophenyl)-2-(2-anilino-4-oxo-4.5-dihvdro-13-thiazol-5- -yljacetamide (40.8 mg, 1 eq) was taken up in HO Ac (2 mL), transferred to a micro-tube and run at 100 °C for 600 s. The reaction mixture was evaporated to give 42. mg, as a crude brown oil. Purified by HP-LCMS, to the pooled fractions was added NaOH (1M) to pH=14, the MeCN was evaporated and the aqueous layer extracted with DCM H20 (9:1), dried and evaporated to give the title compound as an off-white powder: HPLC 99%, RT= 2.02 min (System A, 10-97% MeCN over 3 min), 99%, RT= 0.96 min (System B, 2-95% MeCN over 2 min); Ή NMR (400 MHz, METHANOL-D4) δ ppm 3.23 (m, 1 H) 3.80 (m, 1 H) 4.70 (m, 1 H) 7.02 (m, 1 H) 7.17 (m, 3 H) 7.32 (m, 2 H) 7.50 (m, 2 H) 7.62 (m, 1 H); MS [M+H]+ m/z = 323. 228 METHOD WW Y= H, alkyl
[0861] The thiourea (1.0 eq.) and the oc-bromoester / oc-bromoacid (1.0 eq.) were dissolved in acetone (alternatively water, 1,4-dioxane, THF, 2-propanol or MeCN) and heated at 60-140°C in a sealed tube or by microwave irradiation for 15 - 72 hours. The solvent was removed. And the product purified by crystallization from MeOH or preparative reverse-phase HPLC.
Example 173-2-(Bi(fyclo[2.2.1]hept-2-ylaniino)-l-thia-3-azaspiro[4.4]non-2-en-4-one
[0862] A solution of N-bicyclo[2.2.1]hept-2-ylthiourea (73.9 mg, 0.434 mmol) and methyl 1-bromocyclopentanecarboxylate (89.9 mg, 0.434 mmol) in 1,4-dioxane (600 μΐ,) was stirred at 95 °C in a sealed tube for 20 h. The solvent was removed, and the residue was purified by silica gel flash chromatography (pentane/EtOAc, 6:4). The product-containing fractions were pooled, and the solvent was removed. Subsequent purification of the residue by preparative reverse-phase HPLC yielded the product as a white solid.
[0863] HPLC 100%, RT= 2.98 (System A, 10-97% MeCN over 3 min), 100%, RT= 1.45 min (System B, 2-95% MeCN over 2 min). 108641 1H NMR (400 MHz, DMSO-rf6) δ 1.04-1.19 (m, 3 H), 1.34-1.51 (m, 4 H), 1.59-1.73 (m, 3 H), 1.78-1.99 (m, 4 H), 2.08-2.25 (m, 4 H), 3.18 (m, 0.3 H, minor isomer), 3.77 (m, 0.7 H, major isomer), 9.01 (d, J= 6.7 Hz, 0.7 H, major isomer), 9.68 (s br, 0.3 H, minor isomer).
[0865] MS (ESI+) for C14H2oN2OS m/z 265 (M+H)+. 229 2 METHOD XX
[0867] According to the above synthetic scheme, X of R' 'X is halogen.
[0868] 5-monosubstituted thiazolones may also be further alkylated at the 5-position via the liathiated anion. The following examples illustrate how this methodology can be employed to introduce more complex side-chains.
Example 174-5-(4-Bromobutyl)-2-(cycloheptylamino)-5-methyl-l,3-thiazol-4(5H)-one
[0869] To a continuous N2-flushed solution of 2-(cycloheptylamino)-5-methyl-l,3-thiazol-4(5H)-one hydrobromide (500 mg, 2.2 mmol) in dry THF (50 mL) was added lithium unsopropyiamiae niu oi a zivi soiuuon in mrvnepiane/einyi oenzene, a. a mmoij at - 78°C. The resulting brown solution was allowed to stir lh at this temperature after which time 1,4-dibromobutane (2.1 mL, 17.7 mmol) was added and the solution allowed to warm to -30°C. After lh at this temperature, the reaction was quenched with 6 mL 2/1 MeOH/HOAc and allowed to stir overnight at rt. A saturated solution of aq. NaHC03 was added and the product was extracted with EtOAc and then purified on Si02 (gradient 4/1 - 1/1 hex/EtOAc) to give the bromide as a white solid. Yield 227 mg. HPLC 100% RT=2.34 min (System B, 10-97% MeCN over 3 min), 100% Rr=2.41 min (System A, 10-97% MeCN over 3 min). 1H MR (400 MHz, DMSO-D6) δ ppm 1.15 (td, J=7.20, 3.66 Hz, 1 H) 1.35 - 1.65 (m, 14 H) 1.68 - 1.79 (m, 4 H) 1.82 - 1.91 (m, 2 H) 3.49 (t, J=6.59 Hz, 2 H) 3.95 (dd, J=8.30, 3.91 Hz, 1 H) 9.10 (d, J=7.57 Hz, 1 H). MS(ESI) for C15H25BrN2OS m z 361 (M+H). 230 Example 175-2-(Cycloheptylamino)-5-methyl-5-(4-morpholin-4-yIbutyl)-l,3-thiazol-4(5H)-one
[0870] The bromide intermediate 5-(4-Bromobutyl)-2-(cycloheptylamino)-5-methyl-l,3-thiazol-4(5H)-one (52 mg, 0.14 mmol), described above, was dissolved in THF (3 mL), morpholine (0.84 mmol) added and warmed to 80°C over the weekend. Purification by preprative HPLC and made basic with aq NaHC03, gave the product as a colourless oil. HPLC 100% RT=1.45 min (System B, 10-97% MeCN over 3 min), 100% RT=1.63 min (System A, 10-97% MeCN over 3 min). Ή NMR (400 MHz, DMSO-D6) δ ppm 0.96 - 1.08 (m, 1 H) 1.34 - 1.60 (m, 18 H) 1.82 - 1.90 (m, 2 H) 2.18 (t, J=6.96 Hz, 2 H) 2.24 - 2.32 (m, 4 H) 3.52 (m, 4 H) 3.95 (s, 1 H) 9.08 (br s, 1H). MS(ESI) for Ci9H33N302S m/z 368 (M+H).
METHOD YY Example 176-5-[(dimethyIamino)methyl]-5-methyl-2-[(2-methylphenyl)amino]-l,3-thiazoI-4(5H)-one
[0871] To a solution of {2-[(3-chloro-2-methylphenyl)amino]-4-oxo-4,5-dihydro-l,3-thiazol-5-yl} acetic acid (leq) in 1,4-dioxane was added N,N-dimethylmethyleneiminium chloride (2eq) and the resulting mixture heated in a sealed tube in a microwave reactor at 150°C for 5 minutes. The desired product was then isolated after removal of solvent in vacuo and purification by preperative HPLC. 108721 1H NMR (400 MHz, DMSO-D6) δ ppm 1.42 (s, 3 H) 2.12 (s, 2H) 2.2.3 (s, 6H) 2.57 (d, J=14.0Hz, IE) 2.70 (d, J=14.0Hz, 1H) 3.30 (s, 3H) 6.83 (d, J=7.5Hz, 1H) 7.03 (t, J=7.5Hz, 1H) 7.15 (t, J=7.5Hz, 1H) 7.21 (d, J=7.5Hz, 1H); MS(ESI) for C H19N3OS m/z 278 (M+H). 231
[0873] The following table of compounds were prepared using the methodologiesoutlmed above.
TABLE 2 232 Structure Calc Exp mono Name Method of mono mass Prep. mass 359.1667 359.1662 2-[2- RR (cyclohexylamino)- 4-oxo-4,5-dihydro- l,3-thiazol-5-yl]-N- (2,6- dimethylphenyl)acet amide 359.1667 359.1664 2-[2- KR (cyclohexylamino)- 4-oxo-4,5-dihydro- l,3-thiazol-5-yl]-N- (2,5- dimethylphenyl)acet amide 359.1667 359.1664 2-[2- RR (cyclohexylamino)- 4-oxo-4,5-dihydro- l,3-thiazol-5-yl]-N- (2,4- dimethylphenyl)acet amide 399.0575 399.582 2-[2- RR (cyclohexylamino)- 4-oxo-4,5-dihydro- l,3-thiazol-5-yl]-N- σ (2,5- dichlorophenyl)acet amide 345.1511 345.1552 2-[2- RR (cyclohexylamino)- 4-oxo-4,5-dihydTO- l,3-thiazol-5-yl]-N- (2- methylphenyl)aceta mide 233 234 Structure Calc Exp mono Name Method of mono mass Prep. mass 359.0262 359.0263 N-(2,3- RE. dichlorophenyl)-2- [4-0X0-2- (propylamino)-4,5- di ydro- 1,3-thiazol- 5-yl]acetamide 425.1176 425, 1194 N-(4-chloro-2,5- dimethoxyphenyl)- 2-[2- (cyclohexylamino)- a 4-oxo-4,5-dihydro- l,3-thiazol-5- yl]acetamide 345.1511 345.1514 2-[2- RR (cyclo exylamino)- 4-oxo-4,5-dihydro- l,3-thiazol-5-yl]-N- (4- methylphenyl)aceta mide 409.0419 409.0413 2-[2- RR (bicyclo[2.2.1]hept- 5-en-2-ylamino)-4- H oxo-4,5-dihydro- l,3-thiazol-5-yl]-N- (4- chlorophenyl)aceta mide 409.0419 409.0413 2-[2- RR (bicyclo [2.2.1 ]hept- 5-en-2-ylamino)-4- oxo-4,5-dihydro- a l,3-thiazol-5-yl]-N- (2,5- dichlorophenyl)acet 235 Structure Calc Exp mono Name Method of mono mass Prep. mass amide 283.1718 283.1731 2- UU (cyclooctylamino)- 5-(dimethylamino)- 5-methyl-l,3- thiazol-4(5H)-one 309.1875 309.1S77 2- UU (cycloheptylamino)- 5-methyl-5- piper idin- 1 -y 1- 1 , 3 - thiazol-4(5H)-one 297.1875 297.1868 2- UU (cyclooctylamino)- 5-isopropyl-5- (methylamino)- 1 ,3- thiazol-4(5H)-one '236 237 2H-isoindol-2-yI)-2- oxoethyl]-5-methyl- l,3-thiazol-4(5H)- one ■ 413.2138 413.213697 2- RR (cyclooctylamino)- 5-[2-(3,4- dihydroquinolin- l(2H)-yl)-2- oxoethyl]-5-methyl- l,3-thiazol-4(5H)- one 238 Structure Calc Exp mono Name Method of mono mass Prep. mass 379.1352 379.135447 2-anilino-5-[2-(3,4- RR dihydroquiiiolin- l(2H)-yl)-2- oxoethyl]-5-methyl- l,3-thiazol-4(5H)- one 264.1296 264.1307 2- WW (bicyclo[2.2.1]hept- 2-ylamino)- 1 -thia-3 - azaspiro[4.4]non-2- en-4-one 266.1453 266.1442 2- WW o (cycloheptylamino)- l-thia-3- azaspiro[4.4]non-2 - en-4-one 280.1609 280.1611 2- WW 0 (cyclooctylamino)- 1 -thia-3 - azaspiro[4.4]non-2- en-4-one 266.1453 266.1445 2-[(2,2,3,3- WW tetramethylcyclopro pyl)amino]- 1 -thia-3- azaspiro[4.4]non-2- en-4-one 266.1453 266.146 2- WW (bicyclo[2.2.1]hept- 2-ylamino)-5- methyl-5-propyl- H l,3-thiazol-4(5H)- one 239 240 Structure Calc Exp mono Name Method of mono mass Prep. mass 278.1453 278.1459 5-ethyl-5-methyl-2- WW 0 (tricyclo[3.3.1.0-3,7 ~]non-3-ylamino)- H l,3-thiazol-4(5H)- one 280.1245 278.0941 2-[(lS,2S,4R)- WW bicyclo[2.2.1]hept- 2-ylamino]-8-oxa- 1 - thia-3- azaspiro[4.5]dec-2- en-4-one 252.1296 252.1296 2- WW 0 (bicyclo[2.2.1]hept- l-ylamino)-5-ethyl- 5-methyl-l ,3- thiazol-4(5H)-one 268.1609 268.1601 2- WW (cyclooctylamino)- 5-ethyl-5-methyl- l,3-thiazol-4(5H)- H one 292.1609 292.1614 5 -methyl-5 -propyl- WW 0 2- (tricyclo[3.3.1.0-3,7 ~]non-3-ylamino)- H l,3-thiazol-4(5H)- one 266.1453 266.1443 2- WW (bicyclo[2.2.1]hept- 2-ylamino)-5,5- diethyl-l ,3-thiazol- 4(5H)-one 241 1 242 243 Structure Calc Exp mono Name Method of mono mass Prep. mass 266.1453 266.1445 2- WW (bicyclo[2.2.1]hept- l-ylamino)-5,5- diethyl-l,3-thiazol- 4(5H)-one 266.1453 266.1445 2- WW (bicyclo[2.2.1 ]hept- l-ylamino)-5- methyl-5-propyl- l,3-thiazol-4(5H)- one 360.0871 360.0867 5-(4-bromobutyl)-2- XX (cycloheptylamino)- 5-methyl-l,3- thiazol-4(5H)-one 381.2814 381.281 2- XX (cyclo eptylamino)- 5-[4- (diethylamino)butyl] thiazol-4(5H)-one 367.2293 367.2294 2- XX (cycloheprylarnino)- 5-methyl-5-(4- morpholin-4- ylbutyl)-l ,3-thiazol- 4(5H)-one 380.261 380.2612 2- XX (cycloheptylamino)- 5-methyl-5-[4-(4- methylpiperazin- 1 - yl)butyl]-l,3- thiazol-4(5H)-one 244 245 246 247 248 Structure Calc Exp mono Name Method of mono mass Prep. mass 343. 5-(lH- VV benzimidazol-2- ylmethyl)-2- H [(cyclohexylmethyl) amino]- 1 ,3-thiazol- 4(5H)-one 336.1049 336.1045 2-anilino-5-[( l- VV methyl-lH- benzimidazol-2- yl)methyl]-l ,3- \ thiazol-4(5H)-one 255.1405 255.1397 2-(azepan-l- TT ylamino)-5- isopropyl- 1,3- thiazol-4(5H)-one H 255.1405 255.1401 2-(azepan-l- TT ylamino)-5-ethyl-5- methyl-l,3-thiazol- 4(5H)-one H 267.1405 267.1399 5-ethyl-2- TT (hexahydrocyclopen ta[c]pyrrol-2(lH)- ylamino) - 5 -methy 1- H l,3-rhiazol-4(5H)- one 269.1562 269.157 2-(azepan-l- TT ylamino)-5,5- diethyl-l,3-thiazol- 4(5H)-one H 249 Structure Calc Exp mono Name Method of mono mass Prep. mass 281.1562 281.1569 5,5-diethyl-2- TT (hexahydrocyclopen ta[c]pyrrol-2(lH)- ylamino)-l,3- H thiazol-4(5H)-one 271.1354 271.1344 5-isopropyl-2- TT {[(2 )-2- (methoxymethyl)pyr rolidin- 1 -y 1] amino } - 1 l,3-thiazol-4(5H)- one 271.1354 271.1342 5-isopropyl-2-{[2- TT (methoxymethyl)pyr rolidin-l-yl]amino}- H a-"' l,3-thiazol-4(5H)-/ one 243.1041 243.1049 5-isopropyl-2- TT O (morpholin-4- yhmino)-l,3- thiazoI-4(5H)-one 269.1562 269.1553 2-[(2,6- TT dimethylpiperidin- 1 - yl)amino]-5- isopropyl-1,3- thiazol-4(5H)-one 253.1249 253.1249 5-ethyl-2- TT (hexahydrocyclopen ta[c]pyrrol-2(lH)- y]amino)-l,3- H thiazol-4(5H)-one 250 251 252 Structure Calc Exp mono Name Method of · mono mass Prep. mass 276.1838 276.1844 5-isobutyl-2- SS (tricyclo[3.3.1.0-3,7 ~]non-3-ylamino)- H l,3-oxazol-4(5H)- one 252.1838 252.1828 2- SS (cycloheptylamino)- 5,5-diethyl-l,3- oxazol-4(5H)-one 266.1994 266.1991 2- SS (cyclooctylamino)- 5,5-diethyl-l,3- oxazol-4(5H)-one 250.1681 250.1677 2- SS (bicyclo[2.2.1]hept- 2-ylamino)-5,5- diethyl-l,3-oxazol- 4(5H)-one 276.1838 276.183 5,5-diethyl-2- SS (tricyclo[3.3.1.0-3,7 ~]non-3-ylamino)- l,3-oxazol-4(5H)- one 290.1994 290.1987 2-(l- SS adamantylarnino)- 5,5-diethyl-l,3- oxazoI-4(5H)-one 253 Structure Calc Exp mono Name Method of mono mass Prep. mass 262.1681 262.1675 5-isopropyl-2- SS (tricyclo[3.3.1.0-3,7 ~]non-3-ylamino)- l,3-oxazol-4(5H)- one 278.1994 278.1984 2- SS (cyclooctylarnino)- l-oxa-3- azaspiro[4.5]dec-2- en-4-one trifluoroacetate 276.1838 276.1839 2-(l- SS adamantylamino)-5- isopropyl-1,3- oxazol-4(5H)-one 276.1S3S 276.1832 2-(2- SS adamantylamino)-5- isopropyi-1,3- oxazol-4(5H)-one 292.1787 292.1774 2-[(3-hydroxy-l- SS OH adamanryl)amino] - 5-isopropyl-l,3- oxazol~4(5H)-one 290.1994 290.1995 2-(2- SS adamantylamino)- 5,5-diethyl-l,3- oxazol-4(5H)-one 254 Structure Calc Exp mono Name Method of mono mass Prep. mass 306.1943 306.1953 5,5-diethyl-2-[(3- SS OH ydroxy-1- adamanty])amino]- l ,3-oxazol-4(5H)- one 302.1994 302.1994 2-(2- SS adamantylamino)- 1 - oxa-3- azaspiro[4.5]dec-2- en-4-one 288.1838 288.1833 2-(2- SS adamantylamino)- 1 - oxa-3- azaspiro[4.4 non-2- en-4-one 341.2103 341.2113 8-benzyl-2- SS (cyclohexylamino)- 1- oxa-3,8- diazaspiro[4.5]dec- 2- en-4-one 248.1525 248.1519 2- SS (bicyclo[2.2.1]hept- 2-ylamino)-l-oxa-3- azaspiro[4.4]non-2- en-4-one 264.1838 264.1826 2- SS (cyclooctylamino)- l-oxa-3- azaspiro [4.4]non-2- en-4-one 255 316.1399 316.139 2-(2- SS adamantylamino)-5- methyl-5- (trifluoromethyl)- F l,3-oxazol-4(5H)- one 327.1947 327.1941 8-benzyl-2- SS (cyclopentylamino)- 1- oxa-3,S- diazaspiro[4.5Jdec- 2- en-4-one 256 257 The following tables of compounds are encompassed by the present invention and may be prepared by one of the above methodologies. 258 and R] and R2 are independently defined as hydrogen, Ci-C8 alkyl, CrC8 alkoxy, -NR10R10, - S-(CrC8)alkyl, aryl and heterocyclyl; where R10 independently selected from hydrogen, Ci- C8 alkyl, aryl-CpCg alkyl, d-C8 alkoxy, -S-(C]-C8)alkyl, heterocyclyl and aryl; and any alkyl, alkoxy, heterocyclyl or aryl moiety may be substituted with one to three substituents selected from -halo, unsubstituted C]-C8 alkyl, unsubstituted Ci-C8 alkoxy, unsubstituted C]-C8 thioalkoxy and unsubstituted afyl(CpC4)alkyl. 259 260 261 262 263 IJ64 265 IJ66 267  269 1 270 271 272 273 IJ74 275 276  279 280 P T/US2005/018081 281 PREPARATION OF A PHARMACEUTICAL COMPOSITION EXAMPLE 177: Preparation of tablets Ingredients mg/tablet 1. Active compound of formula 10.0 2. Cellulose, microcrystalline 57.0 3. Calcium hydrogen phosphate 15.0 4. Sodium starch glycolate 5.0 . Silicon dioxide, colloidal 0.25 6. Magnesium stearate 0.75
[0893] The active ingredient 1 is mixed with ingredients 2, 3, 4 and 5 for about 10 minutes. The magnesium stearate is then added, and the resultant mixture is mixed for about 5 minutes and compressed into tablet form with or without film-coating.
[0894] The present invention is not to be limited in scope by the exemplified aspects which are intended as illustrations of single aspects of the invention. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description and accompanying drawings. Such modifications are intended to fall within the scope of the appended claims.
[0895] All references cited herein are hereby incorporated by reference in their 282

Claims (9)

1. 79167/2 CLAIMS: 1. A compound of the general formula (III): wherein: R5 is optionally substituted phenyl-(CR10aR10a)1-3-; and wherein R10a is H, methyl, fluoro or R10a and R10a may combine together to form a C3-C6- cycloalkyl ring; R6 is C1-8-alkyl, Ci-8-alkoxy, C3-i0-cycloalkyl, heterocyclyl, C3-i0-cycloalkyl-Ci. 8-alkyl, CN-Ci-8-alkyl, aryl, aryl-Ci-8-alkyl, heterocyclyl-Ci-8-alkyl or haloalkyl; R7 is -NR8R9, halo, C1-8-alkyl, -(CR8R9)n-OR8, -S-Ci-C8-alkyl, C3-i0-cycloalkyl, heterocyclyl, C3-10-cycloalkyl-C1-8-alkyl, cyano-Ci-8-alkyl, aryl, aryl-C1-8-alkyl, heterocyclyl-C1-8-alkyl, heterocyclyl-C(0)-C1.8-alkyl, heterocyclyl-S02-C1-8- alkyl, Ci-8-haloalkyl, HO-C1-8-alkyl, -C(O)-C3-Ci0-cycloalkyl, -C(0)-C!-C8-haloalkyl, -(CR8R9)n-Y-(CR8R9)n-heterocyclyl or -(CR8R9)n-Y- (CR8R9)n-C(0)-R8, wherein n is 0-5, Y is NR10, 0 or S; wherein any aryl, alkyl, heterocyclyl or cycloalkyl residue is optionally substituted by one or more of -d-Cg-alkyl, -halo, -OH, 283 179167/2 Ci-C8-alkyl-S02-, -S02-aryl, -C(0)-(CR8R9)n-carbamate, -C(0)-0-C1-C8-alkyl, -C(0)-d-C8-alkyl, -C(0)-(CR8R9)n-C(0)-NR8R9, -C(0)-(CR8R9)n-NR8-C(0)-C i -C8-alkyl -C(0)-(CR8R9)n-NR8R9, -C(O)-C3-C10-cycloalkyl, -C(0)-aryl, -C(0)-(CR8R9)n-heterocyclyl, -Ci-C8 alkyl-OR8, -C(0)-halo-C1-C8-alkyl or -C(0)-(CR8R9)n-aryl, wherein any aryl, alkyl, cycloalkyl, or heterocyclyl residue is optionally independently substituted by one or more C1-8-alkyl, aryl, halogen, -NR10R10, Ci-C8-haloalkyl, HO-d-Cg-alkyl, R^^-d-Cs-alkyl, Ci-C8-alkyl-OR10, -OR10, (C3-Ci0)-cycloalkyl, Ci-Cg-alkyl-sulfonyl, -0-(CR8R9)n-heterocyclyl, -O-(CR8R9)n-C(0)-NR8R9, -0-(CR8R9)n-NR8R9, -Y-(CR8R9)n-NR8-C(0)-Ci-C8-alkyl, -Y-(CR8R9)n-heterocyclyl, or CrC8-alkyl-S02; wherein R8 and R9 are each independently hydrogen, d-C8 alkyl, d-C8 alkoxy, -NR10R10, -S-(Ci-C8)alkyl, aryl or heterocyclyl; 284 179167/2 any alkyl, alkoxy, heterocyclyl or aryl may be substituted with one to three substituents being -halo, unsubstituted Ci-C8 alkyl, unsubstituted Ci-C alkoxy, unsubstituted Ci-C8 thioalkoxy or unsubstituted aryl(Ci-C4)alkyl; wherein R10 is independently hydrogen, Ci-C8 alkyl, aryl-Ci-C8 alkyl, Ci-C8 alkoxy, -S-(C!-C8)alkyl, heterocyclyl or aryl; any alkyl, heterocyclyl or aryl may be substituted with one to three substituents being -halo, unsubstituted Ci-C8 alkyl, unsubstituted Ci-C8 alkoxy, unsubstituted Ci-C8 thioalkoxy or unsubstituted aryl(Ci-C4)alkyl; ft 7 or R and R form, together with the carbon atom bonded thereto, a saturated, partially unsaturated or unsaturated C3-i0-cycloalkyl or a saturated, partially unsaturated or unsaturated C4-Ci4 heterocyclyl; wherein the cycloalkyl or the heterocyclyl may be optionally substituted by one or more of CrCs-alkyl, aryl, Ci-C8-haloalkyl, aryl-d-C8-alkyl, C3-Ci0- cycloalkyl, -OR8, =0, =NR8, =N-OR8, -NR8R9, -SR8, -halo, -OC(0)R8, - C(0)R8, -C02R8, -CONR8R9, -OC(0)NR8R9, -NR9C(0)R8, -NR8C(0)NR8R9, - NR8S02NR8R9, -NR8C02R9, -NHC(NH2)=NH, -NR8C(NH2)=NH, - NHC( H2)=NR8, -S(0)R8, -S02R8, -S02NR8R9, -NR8S02R9, -CN or -N02; and pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers and N-oxides thereof, with the proviso that: when R and R combine to form a cyclopropyl ring, then R is not benzyl.
2. The compound of claim 1, wherein R5 is (optionally substituted phenyl)-(C(CH3)2)-, (optionally substituted phenyl)-(CHCH3), or benzyl.
3. A compound of the general formula (III): 285 179167/2 wherein: R5 is Ci-C8 alkyl, C3-1o-cycloalkyl, C3-10-cycloalkyl-Ci-8-alkyl, aryl, aryl-Ci-8- alkyl, heterocyclyl, or haloalkyl; wherein any aryl, cycloalkyl, or heterocyclyl residue is optionally independently substituted by one or more Ci-8-alkyl, aryl, halogen, halo-Ci-Cg-alkyl, HO-Ci-C8- alkyl, R^^-d-d-alkyl, d-Cg-alkyl-OR10, -OR10, (C3-Ci0)-cycloalkyl or C C8- alkyl-sulfonyl; R6 is C!-C8 alkyl, C3-C10 cycloalkyl, saturated or partially unsaturated heterocyclyl, heteroaryl or aryl; R7 is -NR8R9, halo, Ci-g-alkyl, -S-d-Cg-alkyl, C3-10-cycloalkyl, heterocyclyl, C3- 10-cycloalkyl-C1-8-alkyl, cyano-Ci-8-alkyl, aryl, aryl-Ci-g-alkyl, heterocyclyl-Ci-g- alkyl, heterocyclyl-C(0)-C1-8-alkyl, heterocyclyl-S02-C1-8-alkyl, R^^-d-s- alkyl, -C(O)-C3-C10-cycloalkyl, -C(0)-d-C8-haloalkyl, -(CR8R9)n-Y-(CR8R9)n- heterocyclyl or -(CR8R9)n-Y-(CR8R9)n-C(0)-R8 (wherein n is 0-5, Y is NR10, 0 or S); wherein any aryl, alkyl, heterocyclyl or cycloalkyl residue is optionally substituted one or more of -Ci-Cs-alkyl, -halo, d-C8-alkyl-S02-, 286 179167/2 -S02-aryl, -C(0)-(CR8R9)n-carbamate, -C(0)-0-Ci-C8-alkyl, -C(0)-C1-C8-alkyl, -C(0)-(CR8R9)n-C(0)-NR8R9, -C(0)-(CR8R9)n-NR8-C(0)-C1-C8-alkyl -C(0)-(CR8R9)n-NR8R9, -C(O)-C3-C10-cycloalkyl, -C(0)-aryl, -C(0)-(CR8R9)n-heterocyclyl, -d-C8 alkyl-OR8, -C(0)-halo-Ci-C8-alkyl or -C(0)-(CR8R9)n-aryl, wherein any aryl, alkyl, cycloalkyl, or heterocyclyl residue is optionally independently substituted by one or more C1-8-alkyl, aryl, halogen, -NR10R10, Ci- C8-haloalkyl, HO-d-C8-alkyl, R^^-d-Cs-alkyl, d-C8-alkyl-OR10, -OR10, (C3-C10)-cycloalkyl, d-C8-alkyl-sulfonyl, -0-(CR8R9)n-heterocyclyl, -0-(CR8R9)„-C(0)-NR8R9, -0-(CR8R9)n-NR8R9, -Y-(CR8R9)n-NR8-C(0)-d-C8-alkyl, -Y-(CR8R9)n-heterocyclyl, or Ci-C8-alkyl-S02; wherein R and R are each independently hydrogen, d-C8 alkyl, d-C8 alkoxy, - NR10R10, -S-(d-C8)alkyl, aryl or heterocyclyl; any alkyl, alkoxy, heterocyclyl or aryl may be substituted with one to three substituents being from -halo, unsubstituted d-C8 alkyl, unsubstituted d-C8 alkoxy, unsubstituted Ci-C8thioalkoxy and unsubstituted aryl(Ci-C4)alkyl; 287 179167/2 wherein R10 is independently hydrogen, Ci-C8 alkyl, aryl-Ci-C8 alkyl, Cj-C8 alkoxy, -S-(Ci-C8)alkyl, heterocyclyl or aryl; any alkyl, heterocyclyl or aryl may be substituted with one to three substituents being -halo, unsubstituted Cj- alkyl, unsubstituted Ci-C8 alkoxy, unsubstituted Cj-Cg thioalkoxy or unsubstituted aryl(C!-C4)alkyl; 7 or R and R form, together with the carbon atom bonded thereto, a saturated, partially unsaturated or unsaturated C3-10-cycloalkyl or a saturated, partially unsaturated or unsaturated C4-Cj4 heterocyclyl; wherein the cycloalkyl or the heterocyclyl may be optionally substituted by one or more of Ci-C8-alkyl, aryl, Q-Cg-haloalkyl, aryl-d-C8-alkyl, C3-Ci0-cycloalkyl, - OR8, =0, =NR8, =N-OR8, -NR8R9, -SR8, -halo, -OC(0)R8, -C(0)R8, -C02R8, - CONR8R9, -OC(0)NR8R9, -NR9C(0)R8, -NR8C(0)NR8R9, -NR8S02NR8R9, - NR8C02R9, -NHC(NH2)=NH, -NR8C(NH2)=NH, -NHC(NH2)=NR8, -S(0)R8, - S02R8, -S02NR8R9, -NR8S02R9, -CN and -N02; and pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers and N-oxides thereof, with the proviso that: when R =R =methyl, then R is not phenyl or 4-iodophenyl, R6=R7=phenyl, then R5 is not phenyl, and 7 S R and R combine to form a cyclopropyl ring, then R is not n-butyl, cyclohexyl, benzyl, phenyl or naphthyl; or a compound which is 2-(bicyclo[2 ]hept-2-ylammo)-5-isopropyl-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1 ]hept-2-ylamino)-5-ethyl- 1 ,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1]hept-2-ylamino)-5-phenyl-l,3-thiazol-4(5H)-one; 288 179167/2 2-(cyclohexylamino)-5-ethyl- 1 ,3-thiazol-4(5H)-one; 2-(bicyclo[2 ]hept-2-ylamino)-5,5-dimethyl-l,3-thiazol-4(5H)-one; 5- Isopropyl-2-(tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l,3-thiazol-4(5H)-one; 6- (tricyclo[3.3.1.0~3,7~]non-3-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-(Tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l ,3-thiazol-4(5H)-one; 6-(Cyclooctylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-(Cycloheptylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-(Bicyclo[2.2.1]hept-2-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-[(2,2,3,3-Te1xamethylcyclopropyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-[(2-Methylphenyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2- [(cyclohexylmethyl)amino] -5,5 -dimethyl- 1 ,3 -thiazol-4(5H)-one; 2-[(2-fluorophenyl)amino]-5-isopropyl-l,3-thiazol-4(5H)-one; 2-[(cyclohexylmemyl)amino]-5-(2-hydroxyphenyl)-l,3-thiazol-4(5H)-one; (5S)-2-(cycloheptylamino)-5-methyl-l,3-thiazol-4(5H)-one; (5R)-2-(cycloheptylamino)-5-methyl- 1 ,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; 5-/ert-butyl-2-(cycloheptylamino)- 1 ,3 -thiazol-4(5H)-one; 2-(cyclooctylamino)-5-ethyl- 1 ,3-thiazol-4(5H)-one; 5-isopropyl-2-[(2-isopropylphenyl)amino]-l,3-thiazol-4(5H)-one; 5-ethyl-2-[(2-isopropylphenyl)amino]-l,3-thiazol-4(5H)-one; 289 179167/2 2-[(2-chlorophenyl)amino]-5-ethyl-l,3-thiazol-4(5H)-one; 5-ethyl-2-[(2-methylphenyl)amino]-l,3-thiazol-4(5H)-one; 5-isopropyl-2-[(2,2,3,3-tetramethylcyclopropyl)amino]-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1]hept-2-ylamino)-5-(4-hydroxybenzyl)-l,3-thiazol-4(5H)-one; 5-[(cyclohexylmethyl)amino]-4-thia-6-azaspiro[2.4]hept-5-en-7-one; 2-(cycloheptylamino)-5-(3,4-dihydroxybenzyl)-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-( 1 H-imidazol-4-ylmethyl)- 1 ,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-isobutyl-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-( 1 H-indol-3 -ylmethyl)- 1 ,3 -thiazol-4(5H)-one; 2-(cycloheptylamino)-5-(4-hydroxybenzyl)-l,3-thiazol-4(5H)-one; (5i?)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-l,3-thiazol-4(5H)-one; 2-(cyclooctylamino)-5-(4-hydroxybenzyl)-l,3-thiazol-4(5H)-one; (5S)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-l,3-thiazol-4(5H)-one; [2-(cycloheptylamino)-4-oxo-4,5-dihydro-l,3-thiazol-5-yl]acetonitrile; 2-(cycloheptylamino)-5-(^yridin-3-ylmethyl)-l,3-thiazol-4(5H)-one; 5-Isopropyl-2-[(2-methylphenyl)amino]- 1 ,3-thiazol-4(5H)-one; 2-(Cyclooctylamino)-5,5-dimethyl-l,3-thiazol-4(5H)-one; -(Cyclooctylamino)-5-isopropyl- 1 ,3 -thiazol-4(5H)-one; -(Bicyclo [2.2.1 ]hept-2-ylamino)- 1 -thia-3 -azaspiro [4.5] dec-2-en-4-one ; -(Tricyclo[3.3.1.0~3,7~] non-3 -ylamino)-l -thia-3-azaspiro[4.5]dec-2-en-4-one; -(Cycloheptylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 290 179167/2 2-(Cyclooctylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2- { [ 1 -(4-Chlorophenyl)cyclobutyl]amino } -5-isopropyl- 1 ,3 -thiazol-4(5H)-one; 6- { [ 1 -(4-Chlorophenyl)cyclobutyl]amino} -5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-(cycloheptylamino)-5,5-diethyl-l,3-thiazol-4(5H)-one; (5 S)-5-isopropyl-2- { [(2S)-2-phenylpropyl]amino } - 1 ,3 -thiazol-4(5H)-one; (5R)-5-ethyl-2- { [(2S)-2-phenylpropyl]amino} - 1 ,3-thiazol-4(5H)-one; (5S)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5R)-5-isopropyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5S)-5-isopropyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5R)-5-e l-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5S)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; 2-Anilino-5-isopropyl- 1 ,3-thiazol-4(5H)-one; 5-Isopropyl-2-[(2-mo^holin-4-ylemyl)amino]-l,3-trnazol-4(5H)-one; 2-(Bicyclo[2.2.1]hept-2-ylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 2-(Cycloheptylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 2-(Cyclooctylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 2-[(2,2,3,3-Tettamemylcyclopropyl)amino]-l-thia-3-azaspiro[4.4]non-2-en-4-one; or pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides thereof. The compound of claim 3, wherein R6 is Ci-C8 alkyl. 291 179167/2 The compound of claim 4, wherein R6 is methyl, ethyl, n-propyl or iso-propyl. A compound according to Claim 3 which is: 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2. l]hept-2-ylamino)-5-ethyl-l ,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1 ]hept-2-ylamino)-5-phenyl- 1 ,3-thiazol-4(5H)-one; 2-(cyclohexylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1 ]hept-2-ylamino)-5,5-dimethyl- 1 ,3-thiazol-4(5H)-one; 5- Isopropyl-2-(tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l ,3-thiazol-4(5H)-one; 6- (tricyclo[3.3.1.0~3,7~]non-3-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-(Tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l,3-thiazol-4(5H)-one; 6-(Cyclooctylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-(Cycloheptylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-(Bicyclo[2.2.1]hept-2-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-[(2,2,3,3-Tetramethylcyclopropyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 6-[(2-Methylphenyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-[(cyclohexylmethyl)amino]-5,5-dimethyl-l,3-thiazol-4(5H)-one; 2-[(2-fluorophenyl)amino]-5-isopropyl-l,3-thiazol-4(5H)-one; 2-[(cyclohexylmethyl)amino]-5-(2-hydroxyphenyl)-l,3-thiazol-4(5H)-one; (5S)-2-(cycloheptylamino)-5-methyl-l,3-thiazol-4(5H)-one; (5R)-2-(cycloheptylamino)-5-methyl- 1 ,3-thiazol-4(5H)-one; 292 179167/2 2-(cycloheptylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-isopropyl-l,3-thiazol-4(5H)-one; 5-ter/-butyl-2-(cycloheptylamino)-l,3-thiazol-4(5H)-one; 2-(cyclooctylamino)-5-ethyl-l,3-thiazol-4(5H)-one; 5 -isopropyl-2- [(2-i sopropylpheny l)amino] -1,3 -thiazol -4(5 H)-one ; 5-ethyl-2-[(2-isopropylphenyl)amino]-l,3-thiazol-4(5H)-one; 2-[(2-chlorophenyl)amino]-5-ethyl-l,3-thiazol-4(5H)-one; 5-ethyl-2-[(2-methylphenyl)amino]-l,3-thiazol-4(5H)-one; 5-isopropyl-2-[(2,2,3,3-tetramethylcyclopropyl)amino]-l,3-thiazol-4(5H)-one; 2-(bicyclo[2.2.1 ]hept-2-ylamino)-5-(4-hydroxybenzyl)- 1 ,3-thiazol-4(5H)-one; 5- [(cyclohexylmethyl)amino] -4-thia-6-azaspiro [2.4]hept-5-en-7-one; 2-(cyclohep1ylamino)-5-(3,4-dihydroxybenzyl)-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-( 1 H-imidazol-4-ylmethyl)- 1 ,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-isobutyl-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-(lH-indol-3-ylmethyl)-l,3-thiazol-4(5H)-one; 2-(cycloheptylamino)-5-(4-hydroxybenzyl)-l,3-thiazol-4(5H)-one; (57?)-2-(cycloheptylamino)-5-(cyclohexylmetnyl)-l,3-thiazol-4(5H)-one; 2-(cyclooctylamino)-5-(4-hydroxybenzyl)- 1 ,3-thiazol-4(5H)-one; (5S)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-l,3-thiazol-4(5H)-one; [2-(cycloheptylamino)-4-oxo-4,5-dihydro-l,3-thiazol-5-yl]acetonitrile; 2-(cycloheptylamino)-5-(pyridin-3-ylmethyl)-l,3-thiazol-4(5H)-one; 293 179167/2 5- Isopropyl-2-[(2-methylphenyl)amino]-l,3-thiazol-4(5H)-one; 2-(Cyclooctylamino)-5,5-dimethyl-l,3-thiazol-4(5H)-one; 2-(Cyclooctylamino)-5-isopropyl- 1 ,3 -thiazol-4(5H)-one; 2-(Bicyclo[2.2.1 ]hept-2-ylamino)- 1 -thia-3-azaspiro[4.5]dec-2-en-4-one; 2-(Tricyclo[3.3.1.0~3,7~]non-3-ylamino)-l -thia-3-azaspiro[4.5]dec-2-en-4-one; 2-(Cycloheptylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2-(Cyclooctylamino)-l-thia-3-azaspiro[4.5]dec-2-en-4-one; 2- { [ 1 -(4-Chlorophenyl)cyclobutyl] amino} -5-isopropyl- 1 ,3-thiazol-4(5H)-one; 6- {[l-(4-Chlorophenyl)cyclobutyl]amino}-5-thia-7-azaspiro[3.4]oct-6-en-8-one; 2-(cycloheptylamino)-5,5-diethyl-l,3-thiazol-4(5H)-one; (5S)-5-isopropyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5R)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5S)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5R)-5-isopropyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; (5S)-5-isopropyl-2- { [(2R)-2-phenylpropyl]amino} - 1 ,3-thiazol-4(5H)-one; (5R)-5-ethyl-2- { [(2R)-2-phenylpropyl] amino } - 1 ,3 -thiazol-4(5H)-one; (5S)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-l,3-thiazol-4(5H)-one; 2-Anilino-5-isopropyl-l,3-thiazol-4(5H)-one; 5-Isopropyl-2-[(2-morpholin-4-ylemyl)amino]-l,3-tm^ol-4(5H)-one; 2-(Bicyclo[2.2.1]hept-2-ylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 2-(Cycloheptylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 294 179167/2 2-(Cyclooctylamino)-l-thia-3-azaspiro[4.4]non-2-en-4-one; 2-[(2,2,3,3-Tetramethylcyclopropyl)amino]-l-thia-3-azaspiro[4.4]non-2-en-4- one; or pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides thereof. 7. A pharmaceutical formulation comprising a compound as defined in any one of claims 1-6, in combination with a pharmaceutically acceptable diluent or carrier. 8. The pharmaceutical formulation of claim 7, wherein the formulation is formulated for oral delivery. 9. The pharmaceutical formulation of claim 8, wherein the oral delivery is in the form of a tablet. 10. Use of the compound as defined in any one of claims 1 to 6 for the manufacture of a medicament for the prophylaxis or treatment of a 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder or for achieving immuno-modulation. 1 1. The use according to claim 10, wherein the disorder is diabetes, syndrome X, obesity, glaucoma, hyperlipidemia, hyperglycemia, hyperinsulinemia, hypertension, osteoporosis, dementia, depression, virus diseases, or inflammatory diseases. 12. The use according to claim 10 for the treatment or prophylaxis of a medical condition involving delayed or impaired wound healing. 13. The use according to claim 12, wherein the medical condition involving delayed or impaired wound healing is diabetes. 1
4. The use according to claim 12, wherein the medical condition involving delayed or impaired wound healing is caused by treatment with glucocorticoids. 1
5. The use according to claim 12 for the promotion of wound healing in chronic wounds, said wounds being diabetic ulcers, venous ulcers or pressure ulcers. 295 179167/2 1
6. The use according to claim 10, wherein the immuno-modulation is tuberculosis, lepra, or psoriasis. 1
7. Use of the compound as defined in any one of claims 1 to 6 for the manufacture of a medicament for inhibiting 1 1-β-hydroxysteroid dehydrogenase type 1 enzyme in a subject. 1
8. A compound according to claim 3 which is: 2-[l-(4-Fluoro-phenyl)-ethylamino]-5-methyl-5-(tetrahydro-pyran-4-ylmethyl)- thiazol-4-one; (5S)-5-((l-acetyl-4-piperidinyl)methyl)-2-((lS,4R)-bicyclo[2.2.1]hept-2-ylamino)- 5-methyl-l ,3-thiazol-4(5H)-one; (5R)-2-((lS,4R)-bicyclo[2.2.1]hept-2-ylamino)-5-methyl-5-(tetrahydro-2H-pyran-4- ylmethyl)-l,3-thiazol-4(5H)-one; (5S)-2-((lS,4R)-bicyclo[2.2.1]hept-2-ylamino)-5-methyl-5-tetrahydro-2H-pyran-4- yl-l,3-thiazol-4(5H)-one; 296 2-((lR,2R,4S)-bicyclo[2.2.1]hept-2-ylamino)-8-oxa-l-thia-3-azaspiro[4.5]dec-2-en- 4-one; (5S)-2-((lS,4R)-bicyclo[2.2.1]hept-2-ylamino)-5-((l-(3-furanylcarbonyl)-4- piperidinyl)methyl)-5-methyl-l,3-thiazol-4(5H)-one; 2-(l-Cyclohexyl-ethylamino)-5-isopropyl-5-methyl-thiazol-4-one; 2-(5,5-Difluoro-bicyclo[2 .1]hept-2-ylamino)-5-isopropyl-5-methyl-thiazol-4-one; 2-(bicyclo[2 .1]hept-2-ylamino)-5-isopropyl-5-methyl-thiazol-4-one; 2-[l-(2-Trifluoromethyl-phenyl)-ethylamino]-8-oxa-l-thia-3-aza-spiro[4.5]dec-2- en-4-one; (5R)-2-((lS,2S,4R)-bicyclo[2 .1]hept-2-ylamino)-5-methyl-5-(trifluoromethyl)- l,3-thiazol-4(5H)-one; 2-(Bicyclo[2 .1]hept-2-ylamino)-5-(l-fluoro-l-methyl-e1hyl)-5-methyl-thiazol-4- one; 2- [ 1 -(4-Fluoro-phenyl)-ethylamino] -5 -methyl-5 -pyridin-4-yl-thiazol-4-one ; 5-Methyl-5-pyridin-4-yl-2-[l-(2-trifluoromethyl-phenyl)-ethylamino]-thiazol-4-one; 2-[l-(2-Fluoro-phenyl)-ethylamino]-5-methyl-5-pyridin-4-yl-thiazol-4-one; 5-(l -Fluoro- 1 -methyl-ethyl)-2-[ 1 -(2-fluoro-phenyl)-ethylamino]-5-methyl-thiazol- 4-one; 2-[l-(2-Fluoro-phenyl)-ethylamino]-5-methyl-5-trifluoromethyl-thiazol-4-one; 5-(l,l-Difluoro-ethyl)-2-[l-(4-fluoro-phenyl)-ethylamino]-5-methyl-thiazol-4-one; -[l-(2-CUoro-phenyl)-ethylamino]-5-methyl-5-trifluoromethyl-thiazol-4-one; -[l-(4-Fluoro-phenyl)-ethylamino]-5-methyl-5-trifluoromethyl-thiazol-4-one; 297 179167/1 2-[l-(4-Fluoro-phenyl)-ethylamino]-5-(2-methoxy-pyridin-4-yl)-5-methyl-thiazol-4- one; 5-(l-Fluoro-l-methyl-emyl)-2-[l-(4-fluoro-phenyl)-emylamino]-5-methyl-tlnazol- 4- one, (S)-2-((l R,2R,4R)-5-hydroxybicyclo[2.2.1 ]heptan-2-ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one (S)-2-((lR,2S,4R)-5-hydroxybicyclo[2.2.1]heptan-2-ylamino)-5- isopropyl-5- methylthiazol-4(5H)-one, (S)-2-((lS,2S,4R)-6-hydroxybicyclo[2.2.1]heptan-2-ylamino)-5- isopropyl-5- methylthiazol-4(5H)-one, (S)-2-((lS,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-((R)-l- hydroxypropan-2-yl)- 5- methylthiazol-4(5H)-one, (S)-2-((l S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-((S)-l- hydroxypropan-2-yl)- 5-methylthiazol-4(5H)-one, (S)-2-((lS,2S,4R)-bicyclo[2 ]heptan-2-ylarrnno)-5-(2-hydroxypropan-2-yl)-5- methylthiazol-4(5H)-one, (S)-2-((lS,2S,4R)-bicyclo[2 ^]heptan-2-ylammo)-5-methyl-5-(prop-l-en-2- yl)thiazol-4(5H)-one, (S)-2-((lR,2S,4R)-5-hydroxybicyclo[2.2.1]heptan-2-ylamino)-5- isopropyl-5- methylthiazol-4(5H)-one, or pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides thereof. 1
9. A process for the preparation of a compound as defined in claim 1 or 3 comprising the following reaction scheme: 298 179167/1 wherein: X is S; and LG is a leaving group. 20. A process for the preparation of pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides of a compound defined in claim 1 or 3, comprising the following reaction scheme: wherein: X is S; and LG is a leaving group; thereby yielding said compound and converting same to said pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides, thereof. 21. The process of claim 19 or 20, wherein the LG is halide, tosylate, mesylate or triflate. 299 179167/1 22. The process of any one of claims 19-21, wherein the chiral base is a chiral lithium base. 23. A compound that is 2-(Cyclooctylamino)-5,5-dimethyl-l ,3-thiazol-4(5H)-one or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof. 24. A compound according to claim 3 that is 5-ethyl-2-[(2-isopropylphenyl)amino]-l,3-thiazol-4(5H)-one or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof. 25. A compound according to claim 3 that is 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-5-methyl-thiazol-4-one or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof. 26. A compound according to claim 3 that is (S)-2-((lR,2R,4R)-5-hydroxybicyclo[2.2.1 ]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof. For the Applicants, REINHOLD COHN AND PARTNERS By: 300
IL179167A 2004-05-24 2006-11-09 Compounds which act on 11bhsd1, pharmaceutical compositions comprising them and their use IL179167A (en)

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