Synthesis of 4-aryl-2,3,6,7-tetrahydro-1H-pyrimido[4,5-b][1,4]-diazepin-6-ones from 4,5-diamino-1H-pyrimidin-6-ones and 1-aryl-3-(dimethylamino)-1-propanones
✍ Scribed by Braulio Insuasty; Jairo Quiroga; Juan Carlos Argoti; Samuel Gómez; Roberto Martínez; Enrique Angeles; Rubén Gabiño; Manuel Nogueras; Adolfo Sánchez
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1998
- Tongue
- English
- Weight
- 202 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
The reaction of 1‐aryl‐3‐(dimethylamino)‐1‐propanones 1 with one equivalent of 4,5‐diamino‐1__H__‐pyrimidin‐6‐ones 2, in acidic medium, leads to the formation of 4‐aryl‐2,3,6,7‐tetrahydro‐1__H__‐pyrimido[4,5‐b]‐[1,4]diazepin‐6‐ones 3. The structure elucidation of the products is based on detail nmr analysis of experiments such as ^13^C, ^1^H and DEPT including selective ^13^C{^1^H} decoupling experiments.
📜 SIMILAR VOLUMES
## Facile Synthesis of 6-Aryl-1,3-dimethyl-5H-pyrimido[4,5b][1,4]diazepine-2,4(1H,3H)-diones. -A new approach to the regioselective synthesis of the title compounds (IV) starting from readily accessible 6-amino-5-benzylideneaminopyrimidines (I) is described. Condensation of compound (I) with diet
## Abstract For Abstract see ChemInform Abstract in Full Text.