Pyridine → HCID 20294040, compound

Participants

Reaction Steps

A suspension of 4-amino-2-bromo-5-methylthiazole hydrobromide (50 mM 13.7 g) in acetic anhydride (100 ml.) was treated dropwise with pyridine (10 ml.) while cooling in an ice bath. After stirring for 1 hr. the reaction mixture was poured onto 20% aqueous sodium acetate (1l.) and the aqueous solution extracted with dichloromethane (3×500 ml.). The combined organic layers were dried and evaporated under reduced pressure to give an oil which crystallised on trituration with ether. The crude product was recrystallized from ethanol to give the title compound (11.7 g, 50%). mp 129° (Found: C, 31.15; H, 3.15; N, 12.3. C6H7BrN2OS requires: C, 30.6; H, 3.0; N, 11.9%).

Provenance & Evidence