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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398337Generated: October 30, 2026

Oxalyl chloride → 4-(4-chloro-2-fluorophenyl)-N,2-dimethylnicotinamide

https://huagongshe.com/reaction/1398337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant4-(4-Chloro-2-fluorophenyl)-2-methylpyridine-3-carboxylic acidHCID 86710335—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(4-chloro-2-fluorophenyl)-N,2-dimethylnicotinamideHCID 8671033627%

Reaction Steps

To a solution of 4-(4-chloro-2-fluorophenyl)-2-methylnicotinic acid (180 mg, 0.678 mmol) in DCM (5 mL) and DMF (0.2 mL) at 0° C., was added oxalyl chloride (0.178 mL, 2.033 mmol). The reaction mixture was stirred for 3 h at RT then diluted with DCM (5 mL) and treated with a solution of methylamine hydrochloride (457 mg, 6.78 mmol) in DCM (5 mL) cooled to 0° C. The mixture was stirred for another 1 h at RT. The solution was extracted with DCM (20 mL), washed with saturated NaHCO3 (2×10 mL) and water (20 mL); dried over Na2SO4 and concentrated under reduced pressure to afford 4-(4-chloro-2-fluorophenyl)-N,2-dimethylnicotinamide (50 mg, 0.179 mmol, 27% yield) as a brown gum. LC/MS, (ESI) m/z 279.2 [(M+H)+, calcd for C14H13ClFN2O 279.1]; LC/MS retention time (method D): tR=0.62 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901305B2
Source datasetuspto-grants-2014_12
ORD IDord-ac5201aebf5c4e909cd4fe699727074c
Source noteuspto-grants-2014_12