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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660568Generated: November 3, 2026

Thiourea → Ethyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1660568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
ReactantEthyl 2-chloro-4-methylpentanoateHCID 20557029—
SolventEthanolHCID 702—
ProductEthyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylateHCID 82443639.7%

Reaction Steps

Utilizing the procedure of Example 1, a mixture of 1.97 g (0.01 mol) of ethyl 2-chloro-4-methyl-pentanoate, 0.76 g (0.01 mol) of thiourea and 30 ml of ethanol was held at reflux for 18 hours. Ethanol was removed under reduced pressure. The residue was crystallized from hexane. The solid precipitates were dissolved in ether. The ether solution was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from benzene-ether to give 0.85 g (39.6%) of ethyl 2-amino-4-isopropyl-5-thiazolecarboxylate, m.p. 173°-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308391
Source datasetuspto-grants-1981_12
ORD IDord-031f732e532d47bab1a6100ae48e1a54
Source noteuspto-grants-1981_12