IE60007B1 - 17beta-substituted -4-aza-5alpha-androstenones and their use as 5alpha-reductase inhibitors - Google Patents

Description

J Ά The present invention is concerned with 17β-substituted 4-aza-5a-androstenones, their preparation and their use as testosterone-5a-reductase inhibitors.

It is well known that certain undesirable physiological manifestations, such as acne vulgaris, seborrhea, female hirsutism, and male pattern baldness and benign prostatic hypertrophy, are the result of hyperandrogenic stimulation caused by an excessive accumulation of testosterone or similar androgenic hormones in the metabolic system.

Early attempts to provide a chemotherapeutic agent to counter the undesirable results of hyperandrogenicity resulted in the discovery of several steroidal antiandrogens having undesirable hormonal activities of their own. The estrogens, for example, not only counteract the effect of the androgens but have a feminizing effect as well. Non-steroidal antiandrogens have also been developed, for example, 4’-nitro-3’-trifluoromethylisobutyranilide [See Neri et al., Endo., Vol. SI, No. 2 (1972)]. However, these products, though devoid of hormonal effects, are peripherally active, competing with the natural androgens for receptor sites, and hence have a tendency to feminize a male host or the male fetus of a female host. it more recently became known that the principal mediator of androgenic activity in some target organs is 5c-dihydrotestosterone, and that it is formed locally in the target organ by the action of testosterone-5c-reductase. It was therefore postulated and has been demonstrated that inhibitors of testosterone-Sc-reductase serve to prevent or lessen symptoms of hyperandrogenic stimulation.

Nayfe et al., [Steroids f 14# 269 (1969)] demonstrated that methyl 4-androsten-3-one-17Bcarboxylate was a testosterone-5a-reductase inhibitor in vitro. Then Voigt and Hsia, Endocrinology, 92, 1216 (1973), Canadian Pat. No. 970,592, demonstrated that the above.ester and the parent free acid# 4-androsten-3-one-17fi-carboxylic acid ar® both active inhibitors of testosfcerone~5c-reductase in vitro® They further demonstrated that topical application of either testosterone or So-dihydrotestosfcerone caused ) 5 enlargement of the female hamster flank organ, an androgen dependent sebaceous structure, However, concomitant administration of 4-androsten-3-one-17e~ carboxylic acid or its methyl ester inhibited the response elicited by testosterone but did not inhibit, the response elicited by 5ci-<3ihydrotestosterone.

These results were interpreted as indicating that the compounds were antiandrogenic by virtue of their ability to inhibit testosterone-5a-reductase.

A number of 4-aza steroid, compounds are known. See, for example, U.S. Pat. Nos. 2,227,876; 3,239,417; 3,264,301; and 3,285,918; French Pat. No. 1,465,544; Doorenbos and Solomons, J. Pharm. Sci. 62, 4, pp. 638-640 (1973); Doorenbos and Brown, J. Pharm. Sci., 60 8, pp. 1234-1235 (1971); and Doorenbos and Kim, J. Pharm. Sci. 63, 4, pp. 620-622 (1974).

Patent Specification No. 48127 discloses inter alia that androstenone compounds of the formula: ί wherein R is hydrogen, methyl or ethyl; R' is hydrogen or methyl; R8’ is hydrogen or 6-methyl; and Z is 8 8 CO-R , where R is C1~4 alkyl; are active as testosterone 5e-reductase inhibitors.

In addition U-S. Patents 4,377,584 and 4,220,775 of Rasmussen et al- describe a group of 4 -aza-17fi-substituted-5e-androstan-3-ones which are said to be useful in the treatment of hyperandrogenic conditions.

SSOwever, none ©£ the documents mentioned above suggests that any of the novel 17e~acyl-4-aza-5c-androsten1—en—3—ones of che presenc invention as defined below would be expected co have ucilicy as highly potent testosterone— 5a-reductase inhibitors.

The present invention provides novel 176acyl-4-aza-5a-androsten-1-en-3-one compounds of the formula: in which R is hydrogen, methyl or ethyl; r2 ig a branched alkyl radical having up to 12 carbon atoms; R' is hydrogen or methyl; R is hydrogen, e-methyl or β-methyl, and R1 is hydrogen, a-methyl or β-methyl.

Preferred compounds have the formula: Q ) * in which R is hydrogen, methyl or ethyl and R3 is branched chain alkyl of from 4-8 carbon atoms.

Representative compounds of the present invention include the following: 17 β-(t-butylcarbony1)-4-aza-4-methyl-5a-androst-1-en3-one; β-(isobutylcarbonyl)-4-aza-4-methvl-5a-androsfc-1-en 3-one; β-(isooctylcarbonyl)-4-aza-4-methyl-5a-androst-1-en 10 3-one; β-(1,1-diethyIbutylcarbonyl)-4-aza-4-methyl-5aandrost-1-en-3-one; β-(neopentylcarbonyl)-4-aza-4-methyl-5a-androst-1en-3-one; 17 B-(t-amylcarbonyl)-4-aza-4-methyl-5α-androst-l-en3-one; β-(t-hexylcarbony1)-4-aza-4-methy1-5a-androst-1-en3-one; and the corresponding compounds wherein the 4-methyl substituent is replaced by a hydrogen atom or an ethy radical.

The novel compounds present invention from the known steroid ester of the are prepared of the formulas Γ ( viz., 17B-(methoxycarbonyl)-4-aza-5a-androstan-3-one, or another 17B-alkoxycarbonyl-4-aza-5a-androstan-3-one compound, which may have the indicated substitution indicated by R', R and R’" , by (A) dehydrogenating the starting material to produce the corresponding compound'containing a double-bond in the 1,2-position of the A-ring, (B) converting the 17substituent into a 17p-acyl substituent and optionally (C) alkylating the A-ring nitrogen to introduce a 4-methvl or 4-ethyl substituent into the A ring. In carrying out the process, it is essential that Stage (A) dehydrogenation of the 1,2-position of the steroid A ring be carried out using a 4-aza-5eandrostane-3-one-compound having no substituent other than hydrogen attached to the A-ring nitrogen., Stage (3) may-consist of one or more chemical steps and if desired may take place before stage (A) or following stage (A) or stage (C).

In a practical method of carrying out this process, the products IA are formed by 1) heating a 17e-alkoxyeaffboftyl-4-a2a-Se6' androstan-3-one compound (III) with a dehydrogenating agent such as benzeneselenic anhydride in refluxing chlorobenzene to form a 17fl-alkoxycarbonyl-4-aza-5aandrost-l-ene-3-one (IV), 2) reacting the latter with sodium hydride under anhydrous conditions in a neutral solvent such as dimethylformamide, 3) contacting the resulting reaction mixture with an alkyl (e.g. methyl or ethyl) iodide to form the corresponding 17fl-alkoxy~ carbonyl-4- alkyl-4-aza~5a-androst-l-en-3-one (V), 4) subsequently hydrolysing the 17fl-alkoxycarbonyl-4alkyl-4-aza~5C"androst-l-en-3-one with a strong base such as aqueous methanolic potassium hydroxide at the reflux temperature, followed by acidification and isolation of the resulting steroidal acid, 17B~carboxy 4-alkyl-4~aza-5a-androst"l-en"3-one (VI), ) converting the steroidal acid to its corresponding 2-pyridylthio ester by refluxing with triphenyl phosphine and 2,28-dipyridyl disulfide in an inert solvent such as toluene and isolating the resulting product, viz· 17β-(2-pyridylthiocarbonyl)-4~alkyl"4-aza~ 5a-androst-1-en-3-one (VII) by chromatography on silica gel, and 6) reacting the pyridylthio ester with an R--Li or an R2MgX (X = Cl, Br) compound such as secbutylmagnesium chloride in tetrahydrofuran to form the desired product 17g-sec-butylcarbonyl-4-alkyl-4-aza5a-androst-1-en-3-one (VIIIA), which is isolated by chromatography on silica gel. When the previous reaction is carried out using an R^MgX or an R"-Li compound other than secbutylmagnesium chloride, the corresponding 17 6-acyl-4-alkyl-4-asa-5a-androst-1-en3-one is prepared, where acyl is R2 carbonyl.

The corresponding 17B-acyl-4aza~5a-androst~l-en-3~one (XVA) is readily prepared from the 17B-(alkoxycarbonyl)-4-aza-5a~androstone~ 3- one (IV) by repeating the above series of reaction steps but omitting Steps 2) and 3), i.e. treatment of the 4-aza-5-c.-androst-l-en-3-one with sodium hydride followed by methyl or ethyl iodide.

In accordance with a further alternative process of preparing the compounds of formula IA having only hydrogen as the sole substituent on the ring A nitrogen# the double bond in the A ring is introduced as the last step of the process. Thus# a 17B-alkoxycarbonyl-4-aza-5G-androstan-3-one (III) is hydrolyzed to the corresponding steroidal acid, 17Bcarboxy-4-aza-5c-androstan-3-one (IX), which in turn is converted to the corresponding pyridylthio ester# 17B (2-pyridylthiocarbonyl) -4"aza-5ci-androstaa-3-one (X) followed by treatment of the ester with an R2MgX or R2Li compound, where R2 is as defined hereinabove to form a 17g-acyl-4-aza-5a-androstan-3-one (XIA) which is dehydrogenated as previously described to produce a compound XIV, 17s-acyl-4-aza-5a-&ndrost-1-en-3-one.

The 15-methyl derivatives, i.e. compounds in which R,,s is methyl, are prepared from known 16-methyl17-acyl-4-methyl-4-aza-5os-androstan-3-ones, e.g. 4,1δβdimethyl-l7g-acetyl-4-aza-5c-androstan-3-one, by known dehydrogenation procedures for 4-methyl-4-aza compounds to produce the corresponding 4,15β-dimethyl-l78-acetyl4- aza-5c-androst-1-en-3-one.

Th© above reactions are schematically represented in the following reaction scheme, in which X is 2-pyridylthio and the other variables are as defined above. ο COOCHj COOCfij COOCH, ί ί Compounds of the present invention, which may be prepared in accordance with the method described above, have been found to be potent antiandrogens by virtue of their ability to specifically inhibit testosterone~5a-reductase and are therefore suitable for treating the hyperandrogenic conditions of acne vulgaris, seborrhoea, and female hirsutism by topical administration, and for treating all of the above conditions as well as benign prostatic hypertrophy, by oral or parenteral administration.

The present invention thus also provides oral, topical and parenteral pharmaceutical formulations for use in administering the active compounds of the present invention.

The compositions containing the compounds of th® present invention as the active ingredient for use in the treatment of benign prostatic hypertrophy can be administered in a wide variety of therapeutic dosage forms in conventional vehicles for systemic administration, as, for example, by oral administration in the form of tablets, capsules, solutions, or suspensions, or by intravenous injection. The daily dosage of the products may be varied over a wide range varying from 50 to 2,000 mg. The compositions are preferably provided in the form of scored tablets containing 5, 10, 25, 50, 100, 150, 250, and 500 mg of the active ingredient for the symptomatic adjustment of th© dosage to the patient to be treated. An effective amount of the drug is ordinarily supplied at a dosage level of from » to 50 mg/kg of body weight per day. Preferably the range is from 1 to 7 mg/kg of body weight per day. These dosages are well below the toxic dose of the product. Capsules containing an active compound of this invention can be prepared by mixing it with lactose and magnesium stearate, calcium stearate, starch, talc, or other carriers, and placing the mixture in gelatin capsules. Tablets may be prepared by mixing the active ingredient with conventional tableting ingredients such as calciuim phosphate, lactose, corn starch or magnesium stearate. The liquid forms are prepared in suitably flavored suspending or dispersing agents such as the synthetic and natural gums, for example, tragacanth, acacia, methylcellulose. 'Other suitable dispersing agents include glycerin.

For parenteral administration, sterile suspensions and solutions are desired. Isotonic preparations, which usually contain suitable preservative, are prepared for intravenous administration.

For the treatment of acne vulgaris, seborrhoea, female hirsutism, the compounds of the present invention are administered in the form of pharmaceutical corpositions comprising the active compound in combination with a pharmacologically acceptable topically administrable carrier.

These topical pharmaceutical compositions may be in the form of a cream, ointment, gel or aerosol formulation suitable for application to the skin. They ordinarily i 3 include 0.1% to 15%, preferably about 5%, of the active compound, based on the total composition. ’ The method of preparing the novel 176-acyl compounds of the present invention, already described above in general terms, is further illustrated by the following Examples EXAMPLE 1 Step A Methyl 3-oxo-4~a2a-5G~androst-l-ene-17β-carboxylate A suspension of. 83.7 g. of methyl 3-oxo-4-aza-5a-androstane-17carboxylate obtained as in U.S. Patent Specification US-A-4 377 584, and 126,5 g of benzeneseleninic anhydride in 2.09 1 of chlorobenzene was heated at reflux for 2 hours. The reflux condenser was switched to a distillation head and the 1*5 mixture was distilled slowly to remove water that had formed in the reaction (2 hours). The solution was evaporated to leave 198 g of wet residue. The residue as a solution in dichloromethane was washed with saturated aqueous NaHCOg solution and saturated NaCl solution, then dried and evaporated to leave 172.4 g. This material was chromatographed on 2.56 kg of silica gel eluting first with dichloromethane (5 1) and then with 4si dichloromethaneacetone. The desired product eluted after 8 litres and amounted to 53.4 g. It vas rinsed with diethyl ether and dried to leave 49.5 g„ m.p. 278-280°C. f Step Β Methyl 4-methy 1-3-oxo-4-aza-Sc-androst-l-ene-l/Bcarboxylate A suspension of 25 g of the product of Step A and 2.25 g of sodium hydride in 500 ml of dry dimethylformamide was stirred under nitrogen for minutes. Methyl iodide (15 ml) was added dropwise and the mixture was stirred for 30 minutes at room temperature. Additional (5 ml) methyl iodide was added and the mixture was heated at 50°C for 2 hours. After cooling the mixture was diluted with water to 2 1. The solid was separated after cooling and amounted to 25.4 g, m.p. 159~161°C.

Step C S—(2-Pyridyl) 4-methyl-3-oxo-4"aza-5a-androst-l-ene1 5 I7fith iocar boxylate____ A suspension of 25 g of the product of Step B in 125 ml of methanol was treated with a solution of KOH (12.5 g) in 12.5 ml of water. After refluxing for 4 hours, the solution was acidified with 6N HCl and then was diluted with water. The crude acid (23.32 g) was separated,, dried and had m.p. 300°C.

The crude, dry acid (23 g), triphenylphosphine (36.45 g) and 2,2'-dipyridyldisulfide (30.4 g) were suspended in 138 ml of toluene with stirring for 3 hours at room temperature. The reaction mixture was directly chromatographed on a column of 4.5 kg of silica gel eluting with 9:1 (v/v) ethyl acetate-acetone to give 20.4 g of the desired product, m.p. 218-220°C.

Continued elution with acetone gave 5.2 g of the methanol addition product, S-(2-pyridyl) la-methoxy 4-methyl-3-OXO-4-aza-Sc-androstane-17fi-thiocarboxylate, m.p, 221-223°C as a by-product. ί S EXAMPLE 2 Proceeding in a similar fashion to that of Example 1 Step C, the product of Step A Sxample 1 was converted into S-(2-pyridyl) 3-oxo-4-aza-5a-androst1-ene-176-thiocarboxylate, m.p. 230-232°C„ EXAMPLE 3 22-Methyl-4-aza2l-nog-5a-chol°l-ene-3,20-dione (first method) To a solution of 7.2 g of the product of Exanple 2, viz.

S-(2-pyridyl)-3-oxo-4-aza-5a~androst-1-ene-176~thiocarboxylate, in 288 ml of tetrahydrofuran was added at -78°C 33.6 ml of 1.3M S-butylmagnesium chloride. After 30 minutes at -78°C the solution came to room temperature and was treated with saturated aqueous NaCl solution. The product was extracted into dichloromethane and was washed with saturated aqueous NaCl solution and 10% aqueous NaOH solution, then dried and concentrated.

The residue was eluted through 430 g of silica gel dichlorosnethane-acetone to give 4.5 g of the product, m.p. 246-249°C.

EXAMPLE 4 When the procedure of Sxample 3 is repeated using S-(2-pyridyl) 4-methyl3-oxo-4"a«a-5e-androst-1ene-17 p-thiocarboxylate and sec-butyl magnesium chloride as the reagents, the product obtained is 4,22-dimethyl4-asa~21-nor-5c-chol-1-en-3-one, m.p. 134-13o°C. n β EXAMPLE 5 22-Methyl-4-aza-21-nor-5c-chol~lene3,20-dione (second method) A solution of 21 g of 22-methyl-4asa-21-nor*i 5a-cholane~3,20-dione and 29.49 g of benzeneseleninic anhydride in 552 ml of chlorobenzene was refluxed with water separation for 4 hours» The mixture was concentrated and the residue was redissolved in diehloromethane. After washing with 10% (w/v) aqueous sodium hydroxide, then 10% (w/v) hydrochloric acid and saturated aqueous sodium chloride,the solution was dried and concentrated to 45 g of yellow residue. This was chromatographed on 1.5 kg of silica gel packed In diehloromethane and eluted with ethyl acetate to give 10.6 g of the product, m.p. 248-251°C.

EXAMPLE 6 Step A The procedure of Example 3 is followed using S-(2-pyridyl) 3-oxo-4-aza-5a-androstene-17B-thiocarboxylate and isobutyl magnesium chloride as reagents.

The product is 23-methyl-4-aza-21-nor-5«-cholane-3,20dione, m.p. 220-222°C.

Step B When the procedure of Example 5 is repeated using 23-methyl-4-aza-21-nor-5a-cholane-3,20-dione, which can be obtained as described in Step A, as starting material, the product obtained is 23-methyl-4aza-21-nor-5a-chol-1-ene-3,20-dione, m.p. 283-286°C.

Claims (11)

1. A compound of the formula: in which R is hydrogen, methyl or ethyl; 5 R 2 is a branched alkyl radical having up to 12 carbon atoms; R f is hydrogen or methyl; R is hydrogen, α-methyl or 6-methyl, and R' is hydrogen, α-methyl or 6-methyl. 10

2., A compound as claimed in Claim 1 having the formula: in which R is hydrogen, methyl or ethyl and R^ is branched chain alkyl of from 4-8 carbon atoms. ft 8

3. 22-Methyl-4-aza-21-nor-5a-chol-1-ene-3,20-dione.

4. 23-Methyl-4-aza-21-nor-5ra-chol-1-ene-3,20-dione.

5. 4,22-Dimethyl-4-aza-21-nor-5a-chol-1 -en-3-one.

6. A compound as claimed in any one of Claims 1 to 5 for use in treating one or more of the hyperandrogenic conditions of acne vulgaris, seborrhoea, female hirsutism and benign prostatic hypertrophy by oral, parenteral or topical administration.

7. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a compound as claimed in any one of Claims 1 to 5.

8. A compound as claimed in Claim 1, substantially as hereinbefore described and exemplified.

9. A process for the preparation of a compound as claimed in Claim 1, substantially as hereinbefore described and exemplified.

10. A compound as claimed in Claim 1, whenever prepared by a process claimed in Claim 9.

11. A pharmaceutical composition according to Claim 7, substantially as hereinbefore described.