Synthesis of 2-aryl-2,3-dihydro-4-styrylpyrimidodiazepines in the reaction of 4,5,6-triaminopyrimidine and 2,4,5,6-tetraaminopyrimidine with diarylidenacetones
✍ Scribed by Braulio Insuasty; Henry Insuasty; Jairo Quiroga; Manuel Nogueras; Adolfo Sánchez; M. Dolores López
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1999
- Tongue
- English
- Weight
- 266 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
New 6‐amino and 6,8‐diamino‐2‐aryl‐2,3‐dihydro‐4‐styryl‐1__H__‐pyrimido[4,5‐b][1,4]diazepines were obtained in the reaction of 2,4,5,6‐tetraaminopyrimidine 1a and 4,5,6‐triaminopyrimidine 1b with one equivalent of the diaryli dene acetones 2 in absolute ethanol with acetic acid as the catalyst. Structure analysis of 6‐amino and 6,8‐diamino‐2‐aryl‐2,3‐dihydro‐4‐styryl‐1__H__‐pyrimido[4,5‐b][1,4]diazepines 3a‐i, determined by detailed nmr measurements, reveals a high regioselectivity of this reaction.
📜 SIMILAR VOLUMES
## Abstract Several new 6‐amino‐ and 6,8‐diamino‐4‐aryl‐2,3‐dihydropyrimido[4,5‐__b__][1,4]diazepines were obtained from the reaction of 4,5,6‐triaminopyrimidine **1a** and 2,4,5,6‐tetraaminopyrimidine **1b** with one equivalent of 3‐dimethylaminopropiophenones **2** in absolute ethanol. Structure
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract The reaction of the tetraaminopyrimidine 1 with the chalcones **2a‐f** yields, in the presence of catalytic amounts of acetic acid, the 1__H__‐pyrimido[4,5‐__b__][1,4]diazepine derivatives **3a‐f.** The cyclization process consists of a condensation reaction and a Michael type addition.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v