4-Aryl-2-anilinopyrimidines and 2,4-dianilinopyrimidines are privileged structures found in many druglike molecules and biologically active compounds. A method for the quick assembly of novel 4-aryl-and 4-anilino-2-(heteroarylamino)pyrimidines via Buchwald-Hartwig N-arylations at elevated temperatur
ChemInform Abstract: Convenient Preparation of 4-Aryl-2-(heteroarylamino)pyrimidines and 4-Anilino-2-(heteroarylamino)pyrimidines.
✍ Scribed by Brian I. Bliss; Feryan Ahmed; Subashree Iyer; Weimin Lin; Joel Walker; He Zhao
- Book ID
- 102056318
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 36 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
It is demonstrated that non‐nucleophilic heteroarylamines undergo Buchwald—Hartwig N‐arylation with 4‐substituted 2‐chloropyrimidines to afford drug‐like derivatives including analogues (VIc,d) of the reverse transcriptase inhibitor dapivirine.
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