A facile one-pot synthesis of novel substituted 1,2,3,4-tetrahydropyrimidines
✍ Scribed by Enamul Karim; Kaushal Kishore; Jai N. Vishwakarma
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2003
- Tongue
- English
- Weight
- 28 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
A facile one‐pot synthesis of 5‐benzoyl‐6‐methylthio‐1,2,3,4‐tetrahydropyrimidines in good yields is reported.
📜 SIMILAR VOLUMES
## Abstract 1‐(Aralkyl/aryl)‐3‐(alkyyaralkyl)‐5‐aroyl‐1,2,3,4‐tetrahydropyrimidines (**2a‐c**) have been synthesized by dethiomethylation of 5‐aroyl‐6‐methylthio‐1,2,3,4‐tetrahydropyrimidines (**1a‐c**). An alternative one‐pot synthetic strategy has been developed for the title compounds **2a‐t** b
## Abstract Bis‐1,2,3,4‐tetrahydropyrimidinylalkanes/benzenes **2a‐f** have been synthesized by the reaction of N,S‐acetals with formaldehyde and diamines. Reaction of pyrazoles **3a** and **3b** with diamines and formaldehyde yield bis‐4,5,6,7‐tetrahydropyrazolo[3,4‐__d__]pyrimidinylalkanes **4a‐b
## Abstract A one‐pot synthesis of __N__‐sulfonyl‐2‐alkylidene‐1,2,3,4‐tetrahydropyrimidines __via__ a highly selective and copper‐catalyzed multicomponent reaction of sulfonyl azides, terminal alkynes and α,β‐unsaturated imines has been developed. The α,β‐unsaturated imine substrates could be gene