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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696725Generated: November 1, 2026

2,6-Difluorobenzoic acid → HCID 24850494, compound

https://huagongshe.com/reaction/1696725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Difluorobenzoic acidHCID 9796—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant5-[5-Methoxy-2-(trifluoromethyl)-1H-benzimidazol-1-yl]pyridin-2-amineHCID 57356906—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChloroformHCID 6212—
ProductHCID 24850494HCID 2485049481%

Reaction Steps

To a solution of 5-(5-methoxy-2-(trifluoromethyl)-1H-benzo[d]imidazol-1-yl)pyridin-2-amine (80 mg, 0.25 mmol) in CHCl3 (10 ml) was added 2,6-difluorobenzoic acid (90 mg, 0.57 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) (240 mg, 1.25 mmol) and 4-dimethylaminopyridine (DMAP) (160 mg, 1.31 mmol). The resultant solution was allowed to stir for 24 hours at room temperature. The reaction progress was monitored by TLC (EtOAc/petroleum ether=1:1). After the completion, the resultant solution was diluted with 30 ml of CHCl3 and washed with 30 ml of H2O. The mixture was dried and concentrated by evaporation under reduced pressure on a rotary evaporator. The crude product was purified by SGC using 1:5 EtOAc/petroleum ether as eluent to afford 90 mg (81%) of 2,6-difluoro-N-(5-(5-methoxy-2-(trifluoromethyl)-1H-benzo[d]imidazol-1-yl)pyridin-2-yl)benzamide (Compound 163) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163777B2
Source datasetuspto-grants-2012_04
ORD IDord-773de39ec4434aca881b3cdbcaa717e4
Source noteuspto-grants-2012_04