Synthesis of mutagenic heteroaromatics: 2-Aminoimidazo (4, 5-f) quinolines.
…， 首藤紘一， 岡本敏彦, T OKAMOTO
Index: Lee; Hashimoto; Shudo; Okamoto Chemical and Pharmaceutical Bulletin, 1982 , vol. 30, # 5 p. 1857 - 1859
Full Text: HTML
Citation Number: 20
Abstract
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
Related Articles:
Synthesis of mutagenic heteroaromatics: 2-Aminoimidazo (4, 5-f) quinolines.
[Chemical and Pharmaceutical Bulletin, , vol. 30, # 5 p. 1857 - 1859]
Synthesis of mutagenic heteroaromatics: 2-Aminoimidazo (4, 5-f) quinolines.
[Chemical and Pharmaceutical Bulletin, , vol. 30, # 5 p. 1857 - 1859]
[Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, , vol. 37, # 2 p. 157 - 159]
Syntheses of 2-Amino-3, 4-dimethyl-3H-imidazo [4, 5-f] quinoline and Its Related Compounds
[Bulletin of the Chemical Society of Japan, , vol. 55, # 7 p. 2233 - 2235]
Synthesis of mutagenic heteroaromatics: 2-Aminoimidazo (4, 5-f) quinolines.
[Chemical and Pharmaceutical Bulletin, , vol. 30, # 5 p. 1857 - 1859]