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Selective nucleophilic substitution reactions in 2,4,6-trisulfanyl-substituted pyrimidine-5-carbonitriles by secondary amines
✍ Scribed by Simon Drescher; Daniel Ramsbeck; Bodo Dobner; Detlef Briel
- Book ID
- 102339250
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 402 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
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The highly functionalized heterocycles 6‐alkyl‐ respectively 6‐aralkylsulfanyl‐2,4‐bis‐(amidomethylsulfanyl) pyrimidine‐5‐carbonitriles react selective in the 2‐position with various secondary cyclic amines under mild conditions. The resulting pyrimidines were finally transformed into the corresponding thieno[2,3‐d]pyrimidine‐6‐carboxylic acid amides which afford the synthesis of selective substituted thienopyrimidines.
📜 SIMILAR VOLUMES
## Abstract Thieno[2,3‐__d__]pyrimidines with benzylsulfanyl and allylsulfanyl group in the presence of other alkylsul‐fanyl substituents react selectively under mild conditions with secondary amines under replacement of the benzyl or allyl residue whereas the other substituents remain intact. This