Synthesis in the phenothiazine series |
| |
Authors: | Z. I. Ermakova A. N. Gritsenko S. V. Zhuravlev |
| |
Affiliation: | (1) Institute of Pharmacology, Academy of Medical Sciences of the USSR, Moscow |
| |
Abstract: | Quaternary salts of imidazo[4,5,1-k,l]phenothiazine were reduced with potassium borohydride to 1,2-dihydro-2-methylimidazo[4,5,1-k,l]phenothiazine, which was converted to 1,2 dihydro-2-methylimidazo[4,5,1-k,l]phenothiazine-1-thione and 1-methylamino-10-formylphenothiazine. The latter was hydrolyzed to 1-methylaminophenothiazine, which was also obtained by reduction of methyl phenothiazine-1-carbamate. The PMR and IR spectra of some of the derivatives are discussed.See [1] for communication XXXV.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 372–374, March, 1974. |
| |
Keywords: | |
本文献已被 SpringerLink 等数据库收录! |
|