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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263128Generated: October 30, 2026

Water → N-(3,4-Dimethylisoxazol-5-yl)-4-(4-phenyl-1,3-thiazol-2-yl)piperidine-1-carboxamide

https://huagongshe.com/reaction/2263128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Phenyl-2-(piperidin-4-yl)thiazoleHCID 24261834—
Reactant2,2,2-Trichloroethyl(3,4-dimethylisoxazol-5-yl)carbamateHCID 86245257—
SolventDimethyl SulfoxideHCID 679—
ProductN-(3,4-Dimethylisoxazol-5-yl)-4-(4-phenyl-1,3-thiazol-2-yl)piperidine-1-carboxamideHCID 11668077—

Reaction Steps

A solution of 2,2,2-trichloroethyl (3,4-dimethylisoxazol-5-yl)carbamate (200 mg, 1.02 mmol), 4-(4-phenyl-1,3-thiazol-2-yl)piperidine (250 mg, 1.02 mmol) and diisopropylethylamine (0.357 ml, 2.05 mmol) in dimethylsulfoxide (4 ml) was stirred at 70° C. for 12 hours, the reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate) to obtain the desired product as a solid. This was recrystallized from a mixed solvent of tetrahydrofuran, ethyl acetate and hexane to obtain the desired product (201 mg, 51.5%) as a solid. mp 156-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-667f533d4b024a33a9dd8c0060801e34
Source noteuspto-grants-2010_12