WHERE R is hydrogen, alkyl of from 1 to 5 carbon atoms, or allyl; R1 is methyl, ethyl, or n-propyl; R2 is alkyl of from 1 to 5 carbon atoms or allyl; and n is 1 or 2, or the pharmacologically acceptable acid addition salts thereof have analgesic activity.
Abstract:
10B - METHYL-13B-ETHYLGON-4,9(11)-DIENES HAVING PROGESTATIONAL AND ANTIESTROGENIC ACTIVITY ARE PREPARED FROM 13B-ETHYLGON-4-ENES BY A SEQUENCE OF REACTIONS, INCLUDING OZONIZATION AT THE 4-POSITION UNSATURATION, INTRODUCTION OF UNSATURATION AT THE 9-POSITION, ADDITION OF A METHYL GROUP AT THE 10-POSITION, AND REFORMATION OF THE A-RING.
Abstract:
WHERE R is hydrogen, alkyl of from 1 to 7 carbon atoms, or allyl; R1 is methyl, ethyl, or n-propyl; R2 is alkyl of from 1 to 7 carbon atoms or allyl; R3 is hydrogen or methyl and n is 1 or 2, or the pharmacologically acceptable acid addition salts thereof have analgesic activity.
Abstract:
13-Aklyl-10-methylgon-4-en-3-ones possessing androgenic, anabolic, progestational activity are prepared from the correspondingly substituted 13-alkyl-10-methylgonan-4-ones wherein groups labile to mesylation are protected to permit selective mesylation of subsequently formed 4-hydroxy group, by converting the 4-one to its 3-hydroxy-methylene derivative, hydrolyzing the oximino group, mesylating the 4-hydroxy group, catalytically hydrogenating the unsaturation at the 4-position, and eliminating the 4-mexyloxy group to form the 4-en-3-one conjugated system.