Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 5-Methyl[1,3]oxazolo[4,5-b]pyridine-2-thiol

5-Methyl[1,3]oxazolo[4,5-b]pyridine-2-thiol synthesis

3synthesis methods
-

Yield:55656-32-1 85%

Reaction Conditions:

Stage #1: carbon disulfide;2-amino-3-hydroxy-6-methylpyridinewith potassium hydroxide in ethanol; for 16 h;Heating / reflux;
Stage #2: with acetic acid in water; pH=5;

Steps:



Methviri.31oxazolor4.5-bipyridine-2-thiol; KOH (14 g, 0.25 mol) was added to a stirred mixture of 2-amino-6-methylpyridin-3-ol (15.5 g, 0.125 mol) in absolute EtOH (500 mL) under an argon atmosphere. Carbon disulfide (16 mL, 0.25 mol) was added and the reaction mixture was heated to reflux in argon for 16 h. The reaction mixture was evaporated to dryness, water (250 mL) was added followed by acetic acid (20 mL) until the pH was ~5. The formed precipitate was separated by filtration, washed with water, and dried to afford 17.7 g (85%) of 5-methyl[1,3]oxazolo[4,5-b]pyridine-2- thiol as a yellow crystalline solid. 1H-NMR-data (DMSO-d6): 7.70 (1H), 7.07 (1H), 2.46 (3H).

References:

WO2006/51410,2006,A1 Location in patent:Page/Page column 39