## 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
Synthesis of 2,3-dihydropyrido- and 2,3-dihydropyrimido-[1,4]diazepines from triaminopyridine and triaminopyrimidine
✍ Scribed by Braulio Insuasty; Alfredo Perez; John Valencia; Jairo Quiroga
- Book ID
- 102338353
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 224 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
The reaction of 2,3,6‐triaminopyridine 1 and 4,5,6‐triaminopyrimidine 2 with one equivalent of the chal‐cones 3, in acetic acid, leads to the formation of the 8‐amino‐2,3‐dihydro‐1__H__‐pyrido[2,3‐b][1,4]diazepine and 6‐amino‐2,3‐dihydro‐1__H__‐pyrimido[4,5‐b][1,4]diazepine derivatives 4 and 5. The products were characterized by NMR techniques such as ^13^C, ^1^H, and DEPT including selective ^13^C{^1^H} decoupling experiments.
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