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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263266Generated: October 26, 2026

Water → N-[6-(Acetylamino)pyridin-3-yl]-4-[4-(2,3-difluorophenyl)-1,3-thiazol-2-yl]piperazine-1-carboxamide

https://huagongshe.com/reaction/2263266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-[4-(2,3-Difluorophenyl)-1,3-thiazol-2-yl]piperazineHCID 68776289—
Reactant2,2,2-Trichloroethyl[6-(acetylamino)pyridin-3-yl]carbamateHCID 86245259—
SolventDimethyl SulfoxideHCID 679—
ProductN-[6-(Acetylamino)pyridin-3-yl]-4-[4-(2,3-difluorophenyl)-1,3-thiazol-2-yl]piperazine-1-carboxamideHCID 6877858636.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2,2,2-trichloroethyl [6-(acetylamino)pyridin-3-yl]carbamate (255 mg, 0.782 mmol), 1-[4-(2,3-difluorophenyl)-1,3-thiazol-2-yl]piperazine (200 mg, 0.711 mmol) and diisopropylethylamine (0.248 ml, 1.42 mmol) in dimethyl sulfoxide (2.5 ml) was stirred at 70° C. for 15 hours. Water was poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with water, and dried over magnesium sulfate anhydrous, and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 119 mg (36.6%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-953e60912b1a4915ae3b8791bd2eb1c3
Source noteuspto-grants-2010_12