Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398439Generated: November 2, 2026

1,2-Dichloroethane → HCID 86710419, compound

https://huagongshe.com/reaction/1398439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHCID 86710420HCID 86710420—
SolventDimethylformamideHCID 6228—
ProductHCID 86710419HCID 8671041952.8%

Reaction Steps

To the stirred solution of 4-(4-chloro-2,5-difluorophenyl)-2-methylnicotinic acid (1.7 g, 4.02 mmol) in DMF (0.5 mL) was added DIEA (2.81 mL, 16.06 mmol), HOBT (1.230 g, 8.03 mmol), EDC (1.155 g, 6.02 mmol) at 0° C. followed by addition of methylamine hydrochloride (0.488 g, 7.23 mmol). After stirring for 10 min, the ice bath was removed and the reaction mixture was allowed to stir overnight. The reaction mixture was concentrated under reduced pressure. The residue was diluted with ethyl acetate (10 mL) and washed with water (10 mL) followed by brine (10 mL). The organic layer was separated and dried over sodium sulphate, filtered, and concentrated under reduced pressure to afford 4-(4-chloro-2,5-difluorophenyl)-N,2-dimethylnicotinamide (1 g, 2.123 mmol, 53% crude yield) as a brown solid which was taken to the next step without purification. LC/MS (ESI) m/e 297.3 [(M+H)+, calcd for C14H12ClF2N2O 297.1]; LC/MS retention time (method B): tR=0.76 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901305B2
Source datasetuspto-grants-2014_12
ORD IDord-0df27f30549547e7b8d264071482baac
Source noteuspto-grants-2014_12