Abstract:
13-ALKYL-17X-SUBSTITUTED - 17 - HYDROXYGON-4-EN-3-ONE, SEMICARBAXONES AND THIOSEMICARBAZONES, $4,6,8(14),9 AND 11 DEHYDRO ANALOGS, AND D-HOMO ANALOGS THEREOF, OPTIONALLY SUBSTITUTED BY METHYL AT POSTIONS 1,2,4,6,7 AND 11, ALKANOYL AT POSTION 17, BY ALKYL, ARYL, ARYLALKYL AND ALKYLARYL IN THE SEMICARBAZONE OR THIOSEMICARBAZONE GROUP, AND BY A 17X-ALKYL GROUP OR BY METHYL OR HAOLGEN IN A 17X-ETHYNYL GROUP (I) ARE PROVIDED BY CONDENSING THE CORRESPONDING 3-KETOSTEROID (II) WITH THE CORRESPONDING SEMICARBAZIDE OR THIOSEMICARBAZIDE (III). COMPOUNDS (I) ARE PHARMACOLOGICALLY ACTIVE IN WARM BLOODED LOWER ANIMALS AS BRONOCHODILATORS AND AS ANTI-INFLAMMATORY AGENTS.
Abstract:
NOVEL 19-NORSTEROIDAL 3-CHLORO-3,5-DIENES, PARTICULARLY, 3-CHLORO-13-ETHYL-17A-ETHYNYL(OR CHLOROETHYNYL)GONA-3,5DIEN-17-OLS (I) ARE PROVIDED BY CHLORO/ENOLIZING THE CORRESPONDING GON-4-EN-3-ONES (II) WITH A REAGENT SUCH AS OXALYL CHLORIDE. COMPOUNDS I ARE PHARMACOLOGICALLY ACTIVE AS BRONOCHODILATORS AND BIOCIDALLY-ACITVE, AS BACTERICIDES.
Abstract:
13 - ALKYL - 17A - AMINOALKYNYL - 3 - CHLOROGONA - 3,5DIEN-17-OLS AND 17-ALKANOATES (1) AND THEIR SALTS ARE USEFUL AS TRICHOMONACIDES, FUNGICIDES, AMEBICIDES AND BACTERICIDES. COMPOUNDS (I) ARE PREPARED BY TREATING THE CORRESPONDING 13 - ALKYL - 3 - CHLORO - 17A - ETHYNLGONA-3,5DIEN-17-OL OR 17-ALKANOTE (II) WITH FORMALDEHYDE AND AN APPROPRIATELY-SUBSTITUTED SECONDARY AMINE.