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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262896Generated: November 2, 2026

Dimethylformamide → Tert-butyl 4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2262896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-Chloro-4-phenylthiazoleHCID 2761359—
SolventWaterHCID 962—
ProductTert-butyl 4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxylateHCID 68777857—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-chloro-4-phenyl-1,3-thiazole (1.16 g, 5.92 mmol), 1-(tert-butoxycarbonyl)-piperazine (3.30 g, 17.8 mmol), potassium carbonate (817 mg, 5.92 mmol) and N,N-dimethylformamide (20 ml) was stirred at 120° C. for 2 hours, poured to water, which was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=7:3) to give the desired product as a solid. The resulting solid was recrystallized from a mixed solvent of hexane and ethyl acetate to yield 1.43 g (70.1%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-f6708f12a54e4d34a6c9fa1c793c85af
Source noteuspto-grants-2010_12