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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630133Generated: October 29, 2026

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

https://huagongshe.com/reaction/630133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantThioureaHCID 2723790—
ReactantEthyl 2-bromo-4-methyl-3-oxopentanoateHCID 13015595—
SolventEthanolHCID 702—
ProductEthyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylateHCID 82443666.4%

Reaction Steps

To a refluxing solution of thiourea (1.9 g, 25.6 mmol) in absolute ethanol (20 mL) was added ethyl 2-bromo-4-methyl-3-oxopentanoate (6.0 g, 25.3 mmol). The solution was stirred at reflux for another 1.5 hours. After cooling to room temperature, the solution was poured in ice/water (100 mL). The mixture was neutralized with concentrated NH4OH. The solid material was recovered by filtration, washed with water (2×20 mL) and hexanes (2×20 mL), and dried in vacuo, affording ethyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylate (3.6 g, 66% yield). The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315521B2
Source datasetuspto-grants-2016_04
ORD IDord-410d14fa27b041738e27adb1a732b1e8
Source noteuspto-grants-2016_04