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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218177Generated: October 25, 2026

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

https://huagongshe.com/reaction/218177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-AminothiazoleHCID 2155—
ReactantPhenyl chloroformateHCID 15891—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Productphenyl N-(1,3-thiazol-2-yl)carbamateHCID 65114875%

Reaction Steps

To a stirred mixture of 2-aminothiazole (2 g, 20 mmol), pyridine (10 mL), and anhydrous dichloromethane (20 mL) was added phenyl chloroformate (3 mL, 24 mmol) under argon at 0° C. The mixture was stirred at the same temperature for 5 min and at rt overnight before saturated aqueous sodium bicarbonate solution (30 mL) was added slowly. After mixed with heptanes (30 mL), the mixture was stirred for 30 min. The solid was filtered, washed with water (3×3 mL) and then diethylether (3×3 mL), and dried to give phenyl thiazol-2-ylcarbamate (3.4 g, 15 mmol, 75% yield) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198311B2
Source datasetuspto-grants-2012_06
ORD IDord-55cb337be6a64da6b0ebcb892d442c5e
Source noteuspto-grants-2012_06