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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929430Generated: October 31, 2026

Water → 7-bromo-2,2-dimethyl-2H,3H,4H-pyrido(3,2-b)(1,4)oxazin-3-one

https://huagongshe.com/reaction/1929430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-5-bromo-3-hydroxypyridineHCID 11694041—
SolventDimethylformamideHCID 6228—
Product7-bromo-2,2-dimethyl-2H,3H,4H-pyrido(3,2-b)(1,4)oxazin-3-oneHCID 5774204020.6%

Reaction Steps

To a suspension of sodium hydride (60% dispersion in mineral oil, 0.68 g) in N,N-dimethylformamide (15 mL) was added dropwise a solution of 2-amino-5-bromopyridin-3-ol (3.22 g) in N,N-dimethylformamide (25 mL) at room temperature over a period of 10 minutes, and the mixture was stirred at room temperature for 20 minutes. To the mixture was added dropwise ethyl α-bromoisobutyrate (3.32 g) over a period of 20 minutes, and the reaction mixture was stirred at room temperature for 1 hour and at 80° C. for 2 hours. After cooling, to the reaction mixture was added cold water, and the mixture was extracted with ethyl acetate. The organic layer was washed successively water and brine, dried over magnesium sulfate and concentrated in vacuo by a half volume. The precipitates were collected by filtration to give 7-bromo-2,2-dimethyl-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one (0.90 g) was obtained as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188073B2
Source datasetuspto-grants-2012_05
ORD IDord-852a5360b28f46a29adcce880a2b6ee9
Source noteuspto-grants-2012_05