[Synthesis of metabolites of mosapramine. I. Synthesis of alcoholic metabolites]

Autor: Syuji Yuasa, Kenichi Demizu, Chiaki Tashiro
Rok vydání: 1992
Předmět:
Zdroj: Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan. 112(2)
ISSN: 0031-6903
Popis: Four alcoholic metabolites of (+-)-3-chloro-5-[3-(2-oxo-1,2,3,5,6,7,8,8a-octahydroimidazo[1,2-a] pyridine-3-spiro-4'-peperidino)propyl]-10,11-dihydro-5'-dibenz[b,f ] azepine(mosapramine), a new antipsychotic drug, were synthesized in order to determine their chemical structures. A mixture of 10-ethoxy-3-chloro-10,11-dihydro-5H-dibenz[b,f]azepine and 11-ethoxy isomer was used as a starting material. Isomeric intermediates, i.e. 10-oxo-3-chloro-5-(3-chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepine and 11-oxo isomer, were separated by chromatography with silica gel. The metabolites were obtained by NaBH4 reduction of the corresponding 10-oxo or 11-oxo compounds followed by introduction of spiro-piperidine moieties into propyl side chain.
Databáze: OpenAIRE