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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660562Generated: October 31, 2026

Water → Ethyl 2-amino-4-(4-fluorophenyl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1660562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThioureaHCID 2723790—
ReactantEthyl 3-(2-chloro-4-fluorophenyl)-3-oxopropanoateHCID 54191286—
SolventEthanolHCID 702—
ProductEthyl 2-amino-4-(4-fluorophenyl)-1,3-thiazole-5-carboxylateHCID 1280168376%

Reaction Steps

A mixture of 10.5 g (0.05 mole) of ethyl p-fluorobenzoylacetate, 6.7 g (0.05 mole) of sulfuryl chloride and 30 ml. of chloroform was held at reflux for 18 hours and cooled. The chloroform solution was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was distilled to give 10.8 g (88%) of ethyl 2-chloro-(p-fluoro)-benzoylacetate as an oil. A mixture of 10.8 g (0.441 mole) of ethyl 2-chloro-(p-fluoro)-benzoylacetate, 3.36 g (0.0441 mole) of thiourea, 20 ml. of water and 10 ml. of ethanol was held at reflux for 3 hours. Ethanol was removed under reduced pressure. The residue was made basic with saturated sodium bicarbonate. The solid was filtered, washed with water and recrystallized from ethanol to give 8.9 g (76%) of ethyl 2-amino-4-(p-fluorophenyl)-5-thiazolecarboxylate as white prisms, m.p. 205°-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308391
Source datasetuspto-grants-1981_12
ORD IDord-96e8b97765cd4c2294e0a0ae8bcaa783
Source noteuspto-grants-1981_12