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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885675Generated: October 31, 2026

Bromine → 3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde

https://huagongshe.com/reaction/885675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant3-Hydroxy-2-nitropyridineHCID 27057—
Reactant6-Bromo-2-nitropyridin-3-olHCID 21873808—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
Product3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehydeHCID 21873737—

Reaction Steps

6-Bromo-2-nitro-pyridin-3-ol. To a solution of 3-hydroxy-2-nitropyridine (20 g, 140 mmol) in CH3OH (400 mL) was added a solution of 25% NaOCH3 in CH3OH (33.0 mL, 153 mmol). After stirring at RT for 30 min, the reaction mixture was cooled to 0° C. and Br2 (7.2 mL, 140 mmol) added slowly. The mixture was stirred for 30 min, and then was quenched with glacial acetic acid (2.5 mL). The solvent was removed under reduced pressure. A portion of the crude material was purified on SiO2 (50% EtOAc/hexanes) to provide the title compound as a white solid. MS (ESI): exact mass calculated for C5H3BrN2O3, 217.93; m/z not found. 1H NMR (400 MHz, CDCl3): 10.24 (s, 1H), 7.74 (d, J=8.6, 1H), 7.54 (d, J=8.6, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242275B2
Source datasetuspto-grants-2012_08
ORD IDord-e576a2e667b04a6cad05fe3306c37d41
Source noteuspto-grants-2012_08