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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596428Generated: October 30, 2026

Methyl 5-(2-bromoacetyl)furan-2-carboxylate → 2-(4-Methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazole

https://huagongshe.com/reaction/1596428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(2-bromoacetyl)furan-2-carboxylateHCID 14945157—
Reactant4-Methoxy-3-propoxythiobenzamideHCID 18511697—
SolventMethanolHCID 887—
Product2-(4-Methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazoleHCID 1851169879.2%

Reaction Steps

To a solution of 877 mg of 5-(2-bromoacetyl)-2-methoxycarbonylfuran in 40 ml of methanol was added 800 mg of 4-methoxy-3-propoxythiobenzamide, and the mixture was refluxed for 1 hour. The reaction mixture was concentrated approximately ¼, then added diethyl ether. After cooling the solution, a precipitate was collected by filtration and dried to obtain 1.05 g of 2-(4-methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazole as a brown powder. mp. 141.0-142.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291487B1
Source datasetuspto-grants-2001_09
ORD IDord-0002b4595eaa4c519ea61b869aa845cb
Source noteuspto-grants-2001_09