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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260900Generated: November 3, 2026

2-(Bromomethyl)-4-chlorobenzonitrile → 5-Chloro-1-(5-chloro-2-cyanobenzyl)-2-imino-1,2-dihydropyridine-3-carboxamide hydrochloride

https://huagongshe.com/reaction/1260900

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromomethyl)-4-chlorobenzonitrileHCID 12668053—
Reactant2-Amino-5-chloronicotinamideHCID 66876883—
SolventDimethylformamideHCID 6228—
Product5-Chloro-1-(5-chloro-2-cyanobenzyl)-2-imino-1,2-dihydropyridine-3-carboxamide hydrochlorideHCID 686622661.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-amino-5-chloronicotinamide (0.15 g) in N,N-dimethylformamide (3 ml) was added 2-(bromomethyl)-4-chlorobenzonitrile (0.31 g), and the mixture was stirred at 100° C. for 14 hr. The reaction mixture was quenched with saturated aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel chromatography (ethyl acetate:hexane=3:2-4:1). 2N Hydrochloric acid-methanol solution (1 ml) was added to the obtained yellow oil at room temperature, and the obtained precipitate was recrystallized from methanol-ethyl acetate to give the title compound (2 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470859B2
Source datasetuspto-grants-2013_06
ORD IDord-60be1d7ba5074f429f5f7ddd946e1ee2
Source noteuspto-grants-2013_06