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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227516Generated: October 29, 2026

N,N-Dimethylaniline → N-[2,4-dibromo-6-methylpyridin-3-yl]-2-bromoacetamide

https://huagongshe.com/reaction/227516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantBromoacetyl bromideHCID 61147—
Reactant2,4-Dibromo-6-methylpyridin-3-amineHCID 10084238—
SolventDichloromethaneHCID 6344—
ProductN-[2,4-dibromo-6-methylpyridin-3-yl]-2-bromoacetamideHCID 1043027185.3%

Reaction Steps

3-Amino-2,4-dibromo-6-methylpyridine (1.16 g, 4.38 mmol) was dissolved in methylene chloride (10 mL). N,N-dimethylaniline (0.77 g, 6.35 mmol) was added to the solution and then a solution of bromoacetyl bromide (1.03 g, 5.12 mmol) in dichloromethane (2 mL) was added dropwise thereto over 5 minutes with stirring and cooling with ice. After completion of addition, the temperature of the mixture was elevated to room temperature and stirred for 12 hours. The resultant mixture was washed sequentially with water, an aqueous saturated sodium hydrogencarbonate solution, and saturated brine. Subsequently, the mixture was dried over sodium sulfate anhydrate and concentrated under reduced pressure. The residue was crystallized from hexane-acetone, to thereby yield 1.44 g of N-[2,4-dibromo-6-methylpyridin-3-yl]-2-bromoacetamide as colorless crystals (yield 85.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560547B2
Source datasetuspto-grants-2009_07
ORD IDord-e10d395fd8334f6f9e4c64dd0960b3fe
Source noteuspto-grants-2009_07