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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279432Generated: November 3, 2026

2-Aminothiazole → benzyl N-(1,3-thiazol-2-yl)carbamate

https://huagongshe.com/reaction/2279432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Productbenzyl N-(1,3-thiazol-2-yl)carbamateHCID 511363970%

Reaction Steps

To a stirred solution of 2-aminothiazole (AA1-A, 3.0 g, 30.0 mmol) and triethylamine (6.30 mL, 45.0 mmol) at 0° C. was added benzyl chloroformate (5 mL, 36 mmol). The reaction was stirred at RT O/N. The reaction mixture was washed with a saturated aqueous solution of NaHCO3, then water and concentrated to dryness under reduced pressure. The resulting yellow solid was crystallized from ethanol to afford AA1-2 in 70% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133235B2
Source datasetuspto-grants-2015_09
ORD IDord-1b383bf2754e46beb060a6433f482530
Source noteuspto-grants-2015_09