Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5270961 | Tetrahedron Letters | 2009 | 6 Pages |
Abstract
Starting from commercially available 4-amino-2,6-dichloropyrimidine, a practical four steps synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines was developed. This strategy could introduce a diverse set of secondary amines and arylamines to displace the 2- and 4-chloro groups. The products of this route are otherwise difficult to access. In addition, 6-amino arylation was carried out to demonstrate the reactivity and utility of 2-dialkylamino-4-arylamino-6-aminopyrimidines as building blocks for assembling interesting aminopyrimidine molecules.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Chaomin Li, Andrew Rosenau,