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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290650Generated: October 30, 2026

Ethyl 2-aminothiazole-4-carboxylate → Ethyl 2-(alpha-bromoacrylamido)thiazole-4-carboxylate

https://huagongshe.com/reaction/1290650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-aminothiazole-4-carboxylateHCID 73216—
Reactant2-Bromoacrylic acidHCID 82633—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-(alpha-bromoacrylamido)thiazole-4-carboxylateHCID 1787679985.7%

Reaction Steps

To a solution containing 0.688 g of ethyl 2-aminothiazole-4carboxilate (prepared as reported in J.A.C.S. 68,266,1946) and 0.3 g of 2-bromoacrylic acid in 10 ml of dioxane, 0.412 g of N-N'dicyclohexylcarbodiimide were and the mixture was stirred at room temperature overnight. After filtration, the solvent was evaporated in vacuo, the solid residue was dissolved in 50 ml of ethyl acetate, treated with saturated solution of sodium bicarbonate and then with 10% hydrochloric acid. The organic phase was dried over anhydrous sodium sulphate and the solvent evaporated in vacuo. The solid residue was purified by recrystallization from ethanol-water to yield 0.52 g of ethyl 2-(α-bromoacrylamido)thiazole-4-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753629
Source datasetuspto-grants-1998_05
ORD IDord-16b5e6a84296485abc98721cf20967e5
Source noteuspto-grants-1998_05