Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Studies on Diazepines. XVI. Synthesis of Monocyclic 1, 3-Diazepines. (1). Thermolysis of 1, 2-Diazepines formed from Methylpyridine N-Imides
栗田 城治小島 弘一土屋 隆
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キーワード: 2-aminopyridines
ジャーナル フリー

1981 年 29 巻 12 号 p. 3688-3695

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抄録
Thermolysis of various 4- and/or 6-methyl-1, 2-diazepines (12a, b and 18a-e), prepared from pyridine and lutidine N-imides (11 and 17a-d) having a methyl group in the 3-position, gave the corresponding 1, 3-diazepines (13 and 19) and the 2-aminopyridine derivatives (14 and 20), whereas 1, 2-diazepines (9a-d) having no methyl group in the 4- or 6-position gave only the parent N-imides (8) and no 1, 3-diazepines. Heating of the 2, 3-diazabicyclo [3. 2. 0] hepta-3, 6-dienes (21a, b) formed from the corresponding 1, 2-diazepines by irradiation also gave the 1, 3-diazepines (13a and 19b).
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© The Pharmaceutical Society of Japan
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