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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387838Generated: November 1, 2026

Pyridine → phenyl N-(1,3-thiazol-2-yl)carbamate

https://huagongshe.com/reaction/387838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-AminothiazoleHCID 2155—
ReactantPhenyl chloroformateHCID 15891—
ReactantTetrahydrofuran ethyl acetateHCID 21939870—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productphenyl N-(1,3-thiazol-2-yl)carbamateHCID 65114896.2%

Reaction Steps

After dissolving 2-aminothiazole (5.01 g, 50.0 mmol) and pyridine (7.91 g, 100 mmol) in dimethylformamide (50 ml), phenyl chloroformate (8.22 g, 52.5 mmol) was added while cooling on ice, and the mixture was stirred at room temperature for 1 hour. The reaction solution was distributed between an ethyl acetate-tetrahydrofuran mixed solvent and water, the organic layer was washed with water and saturated saline and dried over anhydrous magnesium sulfate, the drying agent was filtered off and the filtrate was distilled off under reduced pressure. After adding ethyl acetate and then hexane to the obtained crude product, the precipitated crystals were filtered out and blow-dried to obtain the title compound (10.6 g, 48.1 mmol, 96%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-c10ee5aea83942f1ab6016b659ed1891
Source noteuspto-grants-2013_02