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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263171Generated: October 27, 2026

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

https://huagongshe.com/reaction/2263171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Methyl-4-phenyl-2-piperazinyl-1,3-thiazoleHCID 17233868—
Reactant2,2,2-Trichloroethyl(3,4-dimethylisoxazol-5-yl)carbamateHCID 86245257—
SolventDimethyl SulfoxideHCID 679—
ProductN-(3,4-Dimethylisoxazol-5-yl)-4-(5-methyl-4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamideHCID 6878279560.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2,2,2-trichloroethyl (3,4-dimethylisoxazol-5-yl)carbamate (244 mg, 0.848 mmol), 1-(5-methyl-4-phenyl-1,3-thiazol-2-yl)piperazine (200 mg, 0.771 mmol) and diisopropylethylamine (0.148 ml, 0.848 mmol) in dimethylsulfoxide (2.6 ml) was stirred at 70° C. for 5 hours. Water was poured into the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of hexane and ethyl acetate to give 186 mg (60.8%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-562fafa39af545aeba84c65415fdb8fc
Source noteuspto-grants-2010_12