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- OGURA HARUO
- School of Pharmaceutical Sciences, Kitasato University
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- SAKAGUCHI MASAKAZU
- School of Pharmaceutical Sciences, Kitasato University
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- TAKEDA KAZUYOSHI
- School of Pharmaceutical Sciences, Kitasato University
Abstract
7-Substituted 1, 3-dimethyl-7H-2, 4, 6-(5H, 6H) pyrrolo [2, 3-d] pyrimidinetriones (IIIa, b, c) were prepared from 6-amino-1, 3-dimethyluracil (I) and ethyl α-bromoacetate. Reactionof I and α-bromo-ketones afforded 6, 7-disubstituted 1, 3-dimethyl-7H-2, 4-pyrrolo-[2, 3-d] pyrimidinediones (IV, V, VI). On the other hand, reaction of 6-mercapto-1, 3-dimethyluracil (VIII) and cc-bromocarbonyl compound afforded thieno [2, 3-d] pyrimidines (X, XI).
Journal
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- Chemical and Pharmaceutical Bulletin
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Chemical and Pharmaceutical Bulletin 20 (2), 404-408, 1972
The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390001204173245056
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- NII Article ID
- 130003766976
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- ISSN
- 13475223
- 00092363
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- Text Lang
- en
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed