摘要:
The present invention concerns a method for manufacturing 1-substituted 1H imidazo[4,5-c]quinolin-4-amine compounds through their corresponding formamides. The invention also concerns new formamide intermediates.
摘要:
The process consists in condensing (2-methyl-6,7,8,9-tetrahydro-4H-pyrido-[1,2-a]pyrimidin-3-yl)-acetaldehyde with 6-fluoro-3-piperidinyl)-1,2-benzisoxazole to yield the intermediate enamine, 3-{2-[4-(6-fluorobenzo[d]isoxazole-3-yl)-piperidin-1-yl]vinyl}-2-methyl-6,7,8,9-tetrahydro-pyrido[1,2,-a]pyrimidin-4-one followed by reduction of such an enamine.
摘要:
The invention relates to a method for manufacturing sertaconazole mononitrate. The invention also relates tcserta-conazole mononitrate that is characterized by it: particle size and to sertaconazole mononitrate monohydrate.
摘要:
The invention relates to a method for manufacturing R-(−)-sertaconazole mononitrate. The invention also relates to R-(−)-sertaconazole mononitrate hemiacetonate.