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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730099Generated: October 26, 2026

Hydrochloric Acid → (2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanone

https://huagongshe.com/reaction/730099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-CyanopyridineHCID 7506—
ReactantSodium HydroxideHCID 14798—
ReactantBoron TrichlorideHCID 25135—
Reactant3,4-DifluoroanilineHCID 77469—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTrichloroethyleneHCID 6575—
Product(2-Amino-4,5-difluoro-phenyl)-pyridin-4-yl-methanoneHCID 2232731727%

Reaction Steps

BCl3 (6.2 ml, 1M in DCM) was added drop wise to 1,2-difluoro-4aminobenzene (0.5 g, 0.004 mol) in trichloroethylene (6.5 ml) at 0° C. and this mixture stirred for 15 min. 4-Cyanopyridine (0.48 g, 0.005 mol) was added and the solution was warmed to RT and stirred for 30 min. The solution was then heated at 80-90° C. for 1 h. The resulting solution was refluxed at 160° C. for 4 hr and stirred at RT over night. 3N HCl was added to the reaction mixture and refluxed at 110° C. for 1.5 h. The reaction mixture was cooled to RT and made basic (pH=12) with 6N NaOH. The reaction mixture was diluted with water and DCM. The resulting two layers were separated and the aqueous layer was extracted with DCM, dried over sodium sulphate and concentrated. The compound was purified by column chromatography using silica gel to yield title compound (0.25 g, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582661B2
Source datasetuspto-grants-2009_09
ORD IDord-b8d2fd37d0f04c0e952233717a3261bd
Source noteuspto-grants-2009_09