| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222368 | Tetrahedron | 2011 | 10 Pages |
Abstract
A microwave assisted Buchwald–Hartwig amination protocol is reported for a series of dihalopyridine precursors. Using this procedure, selective substitution of one halogen by aryl or alkylamines is possible in very short time, usually 30 min. Mild base (K2CO3) can be used successfully, which broadens the substrate scope. The second halogen can then be substituted using alkylamines under nucleophilic substitution condition or via a Suzuki–Miyaura cross-coupling reaction. The target compounds are potential inducers of cardiomyogenesis as innovative approach in regenerative medicine.
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Physical Sciences and Engineering
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Organic Chemistry
