SK11892000A3 - Zlúčeniny a ich použitie ako pozitívnych modulátorov ampa receptora - Google Patents

Zlúčeniny a ich použitie ako pozitívnych modulátorov ampa receptora Download PDF

Info

Publication number: SK11892000A3
Authority: SK; Slovakia
Prior art keywords: alkyl; aryl; benzyl; dioxide; cycloalkyl
Prior art date: 1998-02-18

Application number

SK1189-2000A

Other languages

English (en)

Slovak (sk)

Inventor

Mogens Larsen

Thomas Varming

Claus Mathiesen

Jorgen Schell-Kr�Ger

Gunnar M. Olsen

Tina Holm Johansen

Elsebet Ostergaard Nielsen

Alex Haahr Gouliaev

Original Assignee

Neurosearch A/S

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1998-02-18

Filing date

1999-02-18

Publication date

2001-02-12

1999-02-18 Application filed by Neurosearch A/S filed Critical Neurosearch A/S

2001-02-12 Publication of SK11892000A3 publication Critical patent/SK11892000A3/sk

Links

150000001875 compounds Chemical class 0.000 title claims abstract description 207
102000003678 AMPA Receptors Human genes 0.000 title claims abstract description 23
108090000078 AMPA Receptors Proteins 0.000 title claims abstract description 23
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 165
239000001257 hydrogen Substances 0.000 claims abstract description 163
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 83
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 71
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 69
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 15
125000000217 alkyl group Chemical group 0.000 claims description 553
125000003118 aryl group Chemical group 0.000 claims description 275
238000000034 method Methods 0.000 claims description 267
125000000753 cycloalkyl group Chemical group 0.000 claims description 206
125000003545 alkoxy group Chemical group 0.000 claims description 177
-1 atom hydrogen Chemical class 0.000 claims description 176
229910052736 halogen Inorganic materials 0.000 claims description 174
150000002367 halogens Chemical class 0.000 claims description 174
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 172
125000000623 heterocyclic group Chemical group 0.000 claims description 136
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 130
125000001424 substituent group Chemical group 0.000 claims description 113
125000004356 hydroxy functional group Chemical group O* 0.000 claims description 109
125000000304 alkynyl group Chemical group 0.000 claims description 94
125000003342 alkenyl group Chemical group 0.000 claims description 92
125000001188 haloalkyl group Chemical group 0.000 claims description 67
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 60
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 58
125000004149 thio group Chemical group *S* 0.000 claims description 53
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 50
239000000460 chlorine Substances 0.000 claims description 46
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 46
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 37
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 34
125000004966 cyanoalkyl group Chemical group 0.000 claims description 31
125000004438 haloalkoxy group Chemical group 0.000 claims description 30
PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 claims description 26
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 26
208000035475 disorder Diseases 0.000 claims description 25
125000004429 atom Chemical group 0.000 claims description 24
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 23
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 23
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 23
125000005842 heteroatom Chemical group 0.000 claims description 23
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 22
125000004971 nitroalkyl group Chemical group 0.000 claims description 22
201000010099 disease Diseases 0.000 claims description 21
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 20
238000002360 preparation method Methods 0.000 claims description 19
150000003839 salts Chemical class 0.000 claims description 19
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 18
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 17
125000004093 cyano group Chemical group *C#N 0.000 claims description 16
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 16
125000002837 carbocyclic group Chemical group 0.000 claims description 15
238000011282 treatment Methods 0.000 claims description 15
125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 14
125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 14
208000024827 Alzheimer disease Diseases 0.000 claims description 13
125000003277 amino group Chemical group 0.000 claims description 13
229910052794 bromium Inorganic materials 0.000 claims description 13
125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 13
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 12
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 11
208000026139 Memory disease Diseases 0.000 claims description 11
239000008194 pharmaceutical composition Substances 0.000 claims description 11
LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical compound C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 claims description 10
125000003282 alkyl amino group Chemical group 0.000 claims description 10
125000004414 alkyl thio group Chemical group 0.000 claims description 10
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 10
229910052801 chlorine Inorganic materials 0.000 claims description 10
125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 9
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
FTAHXMZRJCZXDL-UHFFFAOYSA-N 3-piperideine Chemical compound C1CC=CCN1 FTAHXMZRJCZXDL-UHFFFAOYSA-N 0.000 claims description 8
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical group C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 claims description 8
125000001246 bromo group Chemical group Br* 0.000 claims description 8
230000015654 memory Effects 0.000 claims description 8
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 7
210000003169 central nervous system Anatomy 0.000 claims description 7
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 7
230000006735 deficit Effects 0.000 claims description 7
239000003814 drug Substances 0.000 claims description 7
VBKFECXATSSIIS-UHFFFAOYSA-N 3-cyclohexyl-2-methyl-7-morpholin-4-ylsulfonyl-3,4-dihydro-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound C1=C2S(=O)(=O)N(C)C(C3CCCCC3)NC2=CC=C1S(=O)(=O)N1CCOCC1 VBKFECXATSSIIS-UHFFFAOYSA-N 0.000 claims description 6
LNVPUDKWUIASGN-UHFFFAOYSA-N 3-cyclohexyl-3,4,8,9-tetrahydro-2h-[1,4]dioxino[2,3-h][1,2,4]benzothiadiazine 1,1-dioxide Chemical compound N1C2=CC=C3OCCOC3=C2S(=O)(=O)NC1C1CCCCC1 LNVPUDKWUIASGN-UHFFFAOYSA-N 0.000 claims description 6
125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 6
125000002252 acyl group Chemical group 0.000 claims description 6
229910052731 fluorine Inorganic materials 0.000 claims description 6
229910052740 iodine Inorganic materials 0.000 claims description 6
201000003723 learning disability Diseases 0.000 claims description 6
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
QDOQLKXQYLZYEA-UHFFFAOYSA-N (3-cyclohexyl-1,1-dioxo-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazin-8-yl)methanol Chemical compound N1S(=O)(=O)C=2C(CO)=CC=CC=2NC1C1CCCCC1 QDOQLKXQYLZYEA-UHFFFAOYSA-N 0.000 claims description 5
PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 claims description 5
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 5
125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 5
WUMDYVDFUYYKMZ-UHFFFAOYSA-N 3-cyclohexyl-3,4,7,8-tetrahydro-2h-[1,4]dioxino[2,3-g][1,2,4]benzothiadiazine 1,1-dioxide Chemical compound N1C2=CC=3OCCOC=3C=C2S(=O)(=O)NC1C1CCCCC1 WUMDYVDFUYYKMZ-UHFFFAOYSA-N 0.000 claims description 5
125000005330 8 membered heterocyclic group Chemical group 0.000 claims description 5
208000000044 Amnesia Diseases 0.000 claims description 5
208000020358 Learning disease Diseases 0.000 claims description 5
URCISWPLBRCAJO-UHFFFAOYSA-N S(=O)(=O)=C1NS(C2=C(N1)C=CC=C2)(=O)=O Chemical compound S(=O)(=O)=C1NS(C2=C(N1)C=CC=C2)(=O)=O URCISWPLBRCAJO-UHFFFAOYSA-N 0.000 claims description 5
206010039966 Senile dementia Diseases 0.000 claims description 5
208000006011 Stroke Diseases 0.000 claims description 5
125000001309 chloro group Chemical group Cl* 0.000 claims description 5
239000003085 diluting agent Substances 0.000 claims description 5
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
230000006984 memory degeneration Effects 0.000 claims description 5
208000023060 memory loss Diseases 0.000 claims description 5
CASOHOKYBJSFPE-UHFFFAOYSA-N n-(3-cyclohexyl-1,1-dioxo-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazin-7-yl)acetamide Chemical compound N1S(=O)(=O)C2=CC(NC(=O)C)=CC=C2NC1C1CCCCC1 CASOHOKYBJSFPE-UHFFFAOYSA-N 0.000 claims description 5
201000000980 schizophrenia Diseases 0.000 claims description 5
125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims description 4
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 4
125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 4
GCKKMVSMOFCWDO-UHFFFAOYSA-N 3-cyclohexyl-8-pyridin-2-yl-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound C=12S(=O)(=O)NC(C3CCCCC3)NC2=CC=CC=1C1=CC=CC=N1 GCKKMVSMOFCWDO-UHFFFAOYSA-N 0.000 claims description 4
LOCXCZBQYNVQCD-UHFFFAOYSA-N 3-cyclopentyl-7-piperidin-1-ylsulfonyl-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound C=1C=C2NC(C3CCCC3)NS(=O)(=O)C2=CC=1S(=O)(=O)N1CCCCC1 LOCXCZBQYNVQCD-UHFFFAOYSA-N 0.000 claims description 4
125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 claims description 4
206010001605 Alcohol poisoning Diseases 0.000 claims description 4
206010003805 Autism Diseases 0.000 claims description 4
208000020706 Autistic disease Diseases 0.000 claims description 4
201000006474 Brain Ischemia Diseases 0.000 claims description 4
241001465754 Metazoa Species 0.000 claims description 4
208000028017 Psychotic disease Diseases 0.000 claims description 4
201000001880 Sexual dysfunction Diseases 0.000 claims description 4
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 4
230000000747 cardiac effect Effects 0.000 claims description 4
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 4
239000003937 drug carrier Substances 0.000 claims description 4
206010015037 epilepsy Diseases 0.000 claims description 4
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 4
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 4
208000014674 injury Diseases 0.000 claims description 4
208000015122 neurodegenerative disease Diseases 0.000 claims description 4
239000002581 neurotoxin Substances 0.000 claims description 4
125000005574 norbornylene group Chemical group 0.000 claims description 4
239000000546 pharmaceutical excipient Substances 0.000 claims description 4
231100000872 sexual dysfunction Toxicity 0.000 claims description 4
201000009032 substance abuse Diseases 0.000 claims description 4
231100000736 substance abuse Toxicity 0.000 claims description 4
208000011117 substance-related disease Diseases 0.000 claims description 4
229940124530 sulfonamide Drugs 0.000 claims description 4
238000001356 surgical procedure Methods 0.000 claims description 4
230000008733 trauma Effects 0.000 claims description 4
ZRRASWJMRDYRFA-UHFFFAOYSA-N 1-(3-cyclohexyl-1,1-dioxo-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazin-7-yl)ethanol Chemical compound N1S(=O)(=O)C2=CC(C(O)C)=CC=C2NC1C1CCCCC1 ZRRASWJMRDYRFA-UHFFFAOYSA-N 0.000 claims description 3
JURGPCFAAKMAIA-UHFFFAOYSA-N 2-cyclohexyl-1,2,3,4-tetrahydroquinazoline-6-sulfonamide Chemical compound N1CC2=CC(S(=O)(=O)N)=CC=C2NC1C1CCCCC1 JURGPCFAAKMAIA-UHFFFAOYSA-N 0.000 claims description 3
CCCLGUCOGQADHQ-UHFFFAOYSA-N 2-ethyl-2-methyl-3h-1,3-benzoxazin-4-one Chemical compound C1=CC=C2OC(CC)(C)NC(=O)C2=C1 CCCLGUCOGQADHQ-UHFFFAOYSA-N 0.000 claims description 3
MOFJSTXFUSYCDO-UHFFFAOYSA-N 2-methyl-2,3-dihydro-1,3-benzoxazin-4-one Chemical compound C1=CC=C2OC(C)NC(=O)C2=C1 MOFJSTXFUSYCDO-UHFFFAOYSA-N 0.000 claims description 3
BIVGFFFLVZMILM-UHFFFAOYSA-N 2-phenyl-2,3-dihydro-1h-quinazolin-4-one Chemical compound N1C2=CC=CC=C2C(=O)NC1C1=CC=CC=C1 BIVGFFFLVZMILM-UHFFFAOYSA-N 0.000 claims description 3
ZQGCBOWEEAHZJP-UHFFFAOYSA-N 3-(2-methylpropyl)-8-piperidin-1-ylsulfonyl-2,3,4,5-tetrahydro-1$l^{6},2,5-benzothiadiazepine 1,1-dioxide Chemical compound C1=C2S(=O)(=O)NC(CC(C)C)CNC2=CC=C1S(=O)(=O)N1CCCCC1 ZQGCBOWEEAHZJP-UHFFFAOYSA-N 0.000 claims description 3
ISRRWUNTXIBXAA-UHFFFAOYSA-N 3-cyclohexyl-6-(2-methoxyphenyl)-7-methyl-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound COC1=CC=CC=C1C(C(=C1)C)=CC2=C1S(=O)(=O)NC(C1CCCCC1)N2 ISRRWUNTXIBXAA-UHFFFAOYSA-N 0.000 claims description 3
VMEPVEFVUCYDSN-UHFFFAOYSA-N 3-cyclohexyl-6-pyridin-3-yl-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound C=1C=C2S(=O)(=O)NC(C3CCCCC3)NC2=CC=1C1=CC=CN=C1 VMEPVEFVUCYDSN-UHFFFAOYSA-N 0.000 claims description 3
ZJYBPAKREINUPO-UHFFFAOYSA-N 3-cyclohexyl-7-(2-methoxyphenyl)-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound COC1=CC=CC=C1C1=CC=C(NC(NS2(=O)=O)C3CCCCC3)C2=C1 ZJYBPAKREINUPO-UHFFFAOYSA-N 0.000 claims description 3
OXJDOMHSJFVGDD-UHFFFAOYSA-N 3-cyclohexyl-7-(4-methylpiperazin-1-yl)sulfonyl-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound C1CN(C)CCN1S(=O)(=O)C1=CC=C(NC(NS2(=O)=O)C3CCCCC3)C2=C1 OXJDOMHSJFVGDD-UHFFFAOYSA-N 0.000 claims description 3
DJSOQLXTYIGTAN-UHFFFAOYSA-N 3-cyclohexyl-7-(4-methylsulfonylpiperazin-1-yl)sulfonyl-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound C1CN(S(=O)(=O)C)CCN1S(=O)(=O)C1=CC=C(NC(NS2(=O)=O)C3CCCCC3)C2=C1 DJSOQLXTYIGTAN-UHFFFAOYSA-N 0.000 claims description 3
PERVUQCEACNMMX-UHFFFAOYSA-N 3-cyclohexyl-7-pyrrolidin-1-ylsulfonyl-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound C=1C=C2NC(C3CCCCC3)NS(=O)(=O)C2=CC=1S(=O)(=O)N1CCCC1 PERVUQCEACNMMX-UHFFFAOYSA-N 0.000 claims description 3
XCDAUCDJYPFMPQ-UHFFFAOYSA-N 4-oxo-2-(trifluoromethyl)-1h-quinazoline-6-sulfonic acid Chemical compound N1=C(C(F)(F)F)NC(=O)C2=CC(S(=O)(=O)O)=CC=C21 XCDAUCDJYPFMPQ-UHFFFAOYSA-N 0.000 claims description 3
PBSYDJWXTZFDNB-UHFFFAOYSA-N 5,7-dibromo-4h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound N1=CNS(=O)(=O)C2=CC(Br)=CC(Br)=C21 PBSYDJWXTZFDNB-UHFFFAOYSA-N 0.000 claims description 3
230000032683 aging Effects 0.000 claims description 3
125000004445 cyclohaloalkyl Chemical group 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
FZICIDCLEHENHI-UHFFFAOYSA-N n-[1-(3-cyclohexyl-1,1-dioxo-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazin-7-yl)ethylidene]hydroxylamine Chemical compound N1S(=O)(=O)C2=CC(C(=NO)C)=CC=C2NC1C1CCCCC1 FZICIDCLEHENHI-UHFFFAOYSA-N 0.000 claims description 3
PSOPMMVKRIPMTJ-UHFFFAOYSA-N 1-(sulfonylmethyl)piperazine Chemical compound O=S(=O)=CN1CCNCC1 PSOPMMVKRIPMTJ-UHFFFAOYSA-N 0.000 claims description 2
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LTTNPGLVTMWWQN-UHFFFAOYSA-N 3-cyclohexyl-7-(1-methylimidazol-2-yl)-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine 1,1-dioxide Chemical compound CN1C=CN=C1C1=CC=C(NC(NS2(=O)=O)C3CCCCC3)C2=C1 LTTNPGLVTMWWQN-UHFFFAOYSA-N 0.000 claims description 2
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Classifications

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- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/88—Oxygen atoms
- C07D239/90—Oxygen atoms with acyclic radicals attached in position 2 or 3
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
- C07D285/18—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines
- C07D285/20—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems
- C07D285/22—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D285/24—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with oxygen atoms directly attached to the ring sulfur atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
- C07D285/18—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines
- C07D285/20—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems
- C07D285/22—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D285/24—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with oxygen atoms directly attached to the ring sulfur atom
- C07D285/26—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with oxygen atoms directly attached to the ring sulfur atom substituted in position 6 or 7 by sulfamoyl or substituted sulfamoyl radicals
- C07D285/28—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with oxygen atoms directly attached to the ring sulfur atom substituted in position 6 or 7 by sulfamoyl or substituted sulfamoyl radicals with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached in position 3
- 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
- C07D513/04—Ortho-condensed systems

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Veterinary Medicine (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Public Health (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Biomedical Technology (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Psychiatry (AREA)
Addiction (AREA)
Pain & Pain Management (AREA)
Heart & Thoracic Surgery (AREA)
Urology & Nephrology (AREA)
Cardiology (AREA)
Vascular Medicine (AREA)
Psychology (AREA)
Hospice & Palliative Care (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

SK1189-2000A 1998-02-18 1999-02-18 Zlúčeniny a ich použitie ako pozitívnych modulátorov ampa receptora SK11892000A3 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DK22698		1998-02-18
PCT/DK1999/000070 WO1999042456A2 (en)	1998-02-18	1999-02-18	Novel compounds and their use as positive ampa receptor modulators

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SK11892000A3 true SK11892000A3 (sk)	2001-02-12

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EP (1)	EP1071426A2 (xx)
JP (1)	JP2002504481A (xx)
CN (1)	CN1293665A (xx)
AU (1)	AU751384B2 (xx)
CA (1)	CA2320354A1 (xx)
EE (1)	EE200000468A (xx)
HU (1)	HUP0101280A3 (xx)
IL (1)	IL137720A0 (xx)
IS (1)	IS5581A (xx)
NO (1)	NO20004121L (xx)
NZ (1)	NZ506251A (xx)
PL (1)	PL342843A1 (xx)
RU (1)	RU2214405C2 (xx)
SK (1)	SK11892000A3 (xx)
TR (1)	TR200002427T2 (xx)
WO (1)	WO1999042456A2 (xx)
ZA (1)	ZA991301B (xx)

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US7671200B2 (en)	1999-10-27	2010-03-02	Cytokinetics, Inc.	Quinazolinone KSP inhibitors
DE10004572A1 (de)	2000-02-02	2001-08-09	Boehringer Ingelheim Pharma	Neue positive allosterische AMPA-Rezeptor Modulatoren (PAARM), Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
FR2812291B1 (fr) *	2000-07-28	2002-12-13	Adir	Nouveaux derives de benzothiadiazine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
CN1314351A (zh) *	2001-03-22	2001-09-26	刘志红	喹唑啉酮合成方法及具有抗癌作用的一类喹唑啉酮化合物
TWI232863B (en) *	2001-06-11	2005-05-21	Akzo Nobel Nv	Benzoxazepine derivatives
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1999
- 1999-02-18 HU HU0101280A patent/HUP0101280A3/hu unknown
- 1999-02-18 WO PCT/DK1999/000070 patent/WO1999042456A2/en not_active Ceased
- 1999-02-18 CA CA002320354A patent/CA2320354A1/en not_active Abandoned
- 1999-02-18 EP EP99904730A patent/EP1071426A2/en not_active Withdrawn
- 1999-02-18 SK SK1189-2000A patent/SK11892000A3/sk unknown
- 1999-02-18 PL PL99342843A patent/PL342843A1/xx unknown
- 1999-02-18 IL IL13772099A patent/IL137720A0/xx unknown
- 1999-02-18 ZA ZA9901301A patent/ZA991301B/xx unknown
- 1999-02-18 RU RU2000121882/04A patent/RU2214405C2/ru not_active IP Right Cessation
- 1999-02-18 CN CN99804196A patent/CN1293665A/zh active Pending
- 1999-02-18 NZ NZ506251A patent/NZ506251A/xx unknown
- 1999-02-18 EE EEP200000468A patent/EE200000468A/xx unknown
- 1999-02-18 TR TR2000/02427T patent/TR200002427T2/xx unknown
- 1999-02-18 JP JP2000532408A patent/JP2002504481A/ja not_active Withdrawn
- 1999-02-18 AU AU25123/99A patent/AU751384B2/en not_active Ceased
2000
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- 2000-08-17 NO NO20004121A patent/NO20004121L/no unknown

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Publication number	Publication date
RU2214405C2 (ru)	2003-10-20
CN1293665A (zh)	2001-05-02
NO20004121L (no)	2000-10-17
EP1071426A2 (en)	2001-01-31
EE200000468A (et)	2002-04-15
HUP0101280A2 (hu)	2001-10-28
NO20004121D0 (no)	2000-08-17
PL342843A1 (en)	2001-07-16
AU2512399A (en)	1999-09-06
WO1999042456A3 (en)	1999-10-07
ZA991301B (en)	1999-09-13
IL137720A0 (en)	2001-10-31
TR200002427T2 (tr)	2001-01-22
AU751384B2 (en)	2002-08-15
NZ506251A (en)	2003-01-31
HUP0101280A3 (en)	2003-02-28
WO1999042456A2 (en)	1999-08-26
IS5581A (is)	2000-08-04
JP2002504481A (ja)	2002-02-12
CA2320354A1 (en)	1999-08-26

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