Synthesis of mutagenic heteroaromatics: 2-Aminoimidazo (4, 5-f) quinolines.

…， 首藤紘一， 岡本敏彦, T OKAMOTO

文献索引：Lee; Hashimoto; Shudo; Okamoto Chemical and Pharmaceutical Bulletin, 1982 , vol. 30, # 5 p. 1857 - 1859

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被引用次数: 20

摘要

1858 ' _ Vol. 30 (1982) 3a) or SnCl2—HC1 treatment (for 7-methyl-6-methylamino-5—nitroquinoline ; 3b) was successful. The Pd—C-catalyzed reduction in more acidic media (in CHSCOZH) gave a better result. Condensation of amines 4a and 4b with BrCN gave the desired aminoimidazoles