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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642280Generated: October 31, 2026

N-bromobutanimide → 4-Bromo-7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl ester

https://huagongshe.com/reaction/642280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl esterHCID 68426358—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromo-7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl esterHCID 8661735471.3%

Reaction Steps

A mixture of 7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl ester (81 mg, 0.27 mmol), N-bromosuccinimide (50 mg, 0.30 mmol) and benzoyl peroxide (3.2 mg, 0.01 mmol) in carbon tetrachloride (2 mL) was refluxed for 4 h before it was cooled to room temperature and partitioned between dichloromethane and water. The organic layer was washed with saturated aqueous sodium bicarbonate solution, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and dichloromethane to give the title compound as a white solid (73 mg): MS: (+) m/z 376.9, 378.9 (M+1, 79Br/81Br), MS: (−) m/z 377.1, 379.1 (M−1, 79Br/81Br)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696223B2
Source datasetuspto-grants-2010_04
ORD IDord-279de60ecab041da9a5dec2fdb570e75
Source noteuspto-grants-2010_04