Synthesis and reactions of n-methyl-4-(methylthio)thieno[2,3-d]-pyrimidinium salts
✍ Scribed by Hiroshi Maruoka; Fumi Okabe; Kenji Yamagata
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2008
- Tongue
- English
- Weight
- 456 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
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Two methods for the preparation of N‐methyl‐4‐(methylthio)thieno[2,3‐d]pyrimidinium salts 6a,b and 13a,b are described. Treatment of 6a,b and/or 13a,b with active methylene compounds such as malononitrile and ethyl cyanoacetate in the presence of sodium methoxide caused nucleophilic addition followed by elimination of methanethiol, giving the corresponding N‐methyl‐4‐ylidenethieno[2,3‐d]‐pyrimidines 7a,b, 8a,b, 14a,b and 15a,b.
📜 SIMILAR VOLUMES
## Abstract magnified image An efficient one‐pot access for the synthesis of the previously unreported tetracyclic fused pyrimido‐[4″,5″:4′,5′]thieno[3′,2′:4,5]thieno[3,2‐__d__]pyrimidine (**3**) and 1,2,3‐triazine[4″,5″:4′,5′]thieno‐[3′,2′:4,5]thieno‐[3,2‐__d__]‐1,2,3‐triazine (**5**) heteroaroma