Pyridopyrimidines. X. Synthesis of 3-Substituted 2-Thioxo-5,7-dimethylpyrido[2,3-d] pyrimidin-4(3H)-ones and their S-Alkylation Under Phase Transfer Conditions
✍ Scribed by Chaitanya G. Dave; Killol J. Patel
- Book ID
- 102344370
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2001
- Tongue
- English
- Weight
- 43 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
2‐Thioxo‐5,7‐dimethylpyrido[2,3‐d]pyrimidin‐4(3__H__)‐ones 3 were synthesized by the cyclocondensation of 2‐amino‐3‐carbethoxy‐4,6‐dimethylpyridine 1 with methyl‐N‐aryldithiocarbamates 2 and compared with the condensation between 1 and aryl isothiocyanates 4. When a comparative study of N vs S alkylation of ambident 2‐thioxo‐5,7‐dimethylpyrido[2,3‐d]pyrimidin‐4(3__H__)‐ones 3 was carried out under liquid‐liquid and solid‐liquid phase transfer conditions using various alkylating agents 5, the S‐alkylated products 6 were obtained exclusively and selectively.
📜 SIMILAR VOLUMES
## 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 A number of 2‐thioxopyrido[3′,2′:4,5]thieno[3,2‐__H__]pyrimdin‐4(3__H__‐ones (5) have been synthesized by cyclocondensation of 2‐carbethoxy‐3‐amino‐4‐phenyl‐6‐substituted‐thieno[2,3‐__b__]pyridines (3) with various isothiocyanates. Compounds 5 were __S__‐methylated routinely and the rea
## Abstract Compound (I) is readily prepared by an aza‐Wittig reaction.