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ChemicalBook CAS DataBase List OXAZOLO[4,5-B]PYRIDIN-2-AMINE
40926-66-7

OXAZOLO[4,5-B]PYRIDIN-2-AMINE synthesis

2synthesis methods
-

Yield:40926-66-7 80%

Reaction Conditions:

in water; for 0.25 h;Reflux;

Steps:

18.1 3-(4-Fluoro-phenyl)-2-(4-methanesulfonyl-phenyl)-N-oxazolo[4,5-b]pyridin-2-yl-propionamide

Step 1: To a solution of cyanogen bromide (4.5 g, 42 mmol) in H2O (18 mL) was added 2-amino-3-hydroxypyridine (4.5 g, 40.9 mmol) and the resultant reaction mixture was stirred at reflux temperature 15 minutes and then cooled to room temperature. The reaction mixture was neutralized carefully with solid NaHCO3 and diluted with water. The solid was collected, washed 5 times with H2O and dried at 50° C. under vacuum to afford oxazolo[4,5-b]pyridin-2-ylamine (4.42 g, 80%): 1H NMR (300 MHz, DMSO-d6) δ ppm 6.95 (dd, J=7.82, 5.18 Hz, 1H) 7.65 (dd, J=7.82, 1.41 Hz, 1H) 7.91 (s, 2H) 8.08 (dd, J=5.18, 1.41 Hz, 1H).

References:

US2012/149718,2012,A1 Location in patent:Page/Page column 34

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