YAKUGAKU ZASSHI
Online ISSN : 1347-5231
Print ISSN : 0031-6903
ISSN-L : 0031-6903
Benzothiazoles. V
Nitration of 2-Methyl- and 2-Methyl-6-acetylaminobenzothiazoles
水野 義久足立 亀久夫
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1952 年 72 巻 6 号 p. 745-747

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(1) Nitration of 2-methylbenzothiazole gave 6-nitro-2-methylbenzothiazole, m. p. 165° (yield, 83%), along with a small amount of other mononitrobenzothiazole, m. p. 117° (yield, 3.7%). The product of m. p. 117° melted at 96-116° when mixed with 7-nitro-2-methylbenzothiazole, m. p. 120°.
(2) Nitration of 2-methyl-6-acetylaminobenzothiazole gave 7-nitro-6-acetylamino-2-methylbenzothiazole in practically a qantitative yield. No other isomers, especially 5-nitro-6-acetylamino-2-methylbenzothiazole, were obtained.

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© by the PHARMACEUTICAL SOCIETY OF JAPAN
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