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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882943Generated: October 27, 2026

Bromoacetyl bromide → 2-(Bromoacetyl)amino-N-(5-chloropyridin-2-yl)benzamide

https://huagongshe.com/reaction/1882943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
Reactant2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventDiisopropylethylamineHCID 81531—
Product2-(Bromoacetyl)amino-N-(5-chloropyridin-2-yl)benzamideHCID 2190635989.6%

Reaction Steps

To a stirred solution of 2-amino-N-(5-chloropyridin-2-yl)benzamide (1.65 g, 6.66 mmol) in tetrahydrofuran (60 mL)and diisopropylethyl amine (1.28 mL) was added bromoacetyl bromide (0.64 mL, 7.32 mmol) dropwise at 0° C. The reaction mixture was warmed to room temperature and stirred overnight. Diluted the reaction mixture with ethyl acetate (120 mL) and water (50 mL). Separated the organic layer and washed with water (25 mL), saturated sodium bicarbonate (50 mL), 0.2 N hydrochloric acid (25 mL), water (50 m). Dried over sodium sulfate and remove the solvent to get crude product (2.2 g), which was used as such in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759414B2
Source datasetuspto-grants-2004_07
ORD IDord-933fabf2d3824887924239c1c1b25258
Source noteuspto-grants-2004_07