Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10595200 | Bioorganic & Medicinal Chemistry Letters | 2012 | 5 Pages |
Abstract
A convenient and scalable four-step novel route has been developed for the synthesis of rosiglitazone (8), an antidiabetic drug. This multistep route requires 4-fluoro benzaldehyde (4), 2,4-thiazolidinedione (6) and 2-chloro pyridine (1) as key reactants and gives overall better yield of rosiglitazone. In addition, some steps have been accelerated, which leads to an overall time saving of 10Â h.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Dhanaji V. Jawale, Umesh R. Pratap, Ramrao A. Mane,