| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5264055 | Tetrahedron Letters | 2014 | 8 Pages |
Abstract
We describe the straightforward synthesis of 6-substituted-2-aminopyrazolo[1,5-a]pyridines from 2-pyridineacetonitriles by N-amination with O-(mesitylsulfonyl)hydroxylamine and subsequent base-promoted cyclization. This N-amination/intramolecular cyclization reaction allows access to a variety of 6-substituted-2-aminopyrazolo[1,5-a]pyridines in a one-pot procedure, in moderate to good yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yosuke Nishigaya, Kentaro Umei, Eri Yamamoto, Yasushi Kohno, Shigeki Seto,
![First Page Preview: Direct access to 2-aminopyrazolo[1,5-a]pyridines via N-amination/cyclization reactions of 2-pyridineacetonitriles Direct access to 2-aminopyrazolo[1,5-a]pyridines via N-amination/cyclization reactions of 2-pyridineacetonitriles](/preview/png/5264055.png)