Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887755Generated: November 1, 2026

Benzyl Bromide → Methyl 3-bromo-6-(dibenzylamino)pyridine-2-carboxylate

https://huagongshe.com/reaction/887755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 6-amino-3-bromopyridine-2-carboxylateHCID 10657127—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-bromo-6-(dibenzylamino)pyridine-2-carboxylateHCID 5914591773.2%

Reaction Steps

To a suspension of 60% sodium hydride (880 mg, 22.0 mmol) and benzyl bromide (6.24 mL, 52.5 mmol) in N,N-dimethylformamide (80 mL) was added a solution of methyl 6-amino-3-bromopyridine-2-carboxylate (2.42 g, 10.5 mmol) in N,N-dimethylformamide (25 mL) under ice-cooling and the mixture was stirred for 30 min. The reaction solution was diluted with diethyl ether, washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=0/100→20/80) to give the title compound (3.16 g, yield 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247429B2
Source datasetuspto-grants-2012_08
ORD IDord-3ce9316cba1a4fb886aa8db671b1ff2d
Source noteuspto-grants-2012_08