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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263220Generated: October 26, 2026

Water → 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]-N-pyridazin-3-ylpiperidine-1-carboxamide

https://huagongshe.com/reaction/2263220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-[4-(4-Fluorophenyl)-1,3-thiazol-2-yl]piperidineHCID 24261841—
Reactant2,2,2-Trichloroethyl pyridazin-3-ylcarbamateHCID 68576698—
SolventDimethyl SulfoxideHCID 679—
Product4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]-N-pyridazin-3-ylpiperidine-1-carboxamideHCID 6877788158%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2,2,2-trichloroethyl pyridazin-3-ylcarbamate (170 mg, 0.629 mmol), 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]piperidine (150 mg, 0.572 mmol) and diisopropylethylamine (0.199 ml, 1.14 mmol) in dimethylsulfoxide (2.0 ml) was stirred at 70° C. for 6 hours. Water was poured into the reaction solution, 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) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give the desired product (127 mg, 58.0%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-47d2d2924df7413290605dc278750192
Source noteuspto-grants-2010_12