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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900239Generated: October 29, 2026

Potassium Carbonate → 2-Carbamoyl-3-[5-(5-chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-methyl-3H-imidazole-4-carboxylic acid

https://huagongshe.com/reaction/900239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromomethyl-5-(5-chloro-thiophen-2-yl)-isoxazoleHCID 11150146—
Reactant2-Cyano-5-methyl-3H-imidazole-4-carboxylic acid ethyl esterHCID 178470394—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product2-Carbamoyl-3-[5-(5-chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-methyl-3H-imidazole-4-carboxylic acidHCID 22939879—

Reaction Steps

A suspension of 194 mg 2-Cyano-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester, 301 mg 3-Bromomethyl-5-(5-chloro-thiophen-2-yl)-isoxazole and 150 mg K2CO3 in 2 ml DMF was stirred for 5 h at RT. After addition of 2 ml brine the mixture was filtered through a chem elut® cartridge by elution with ethyl acetate and then concentrated under reduced pressure. The residue was then dissolved in 5 ml THF/MeOH/water 3:1:1 and treated with 30 mg LiOH monohydrate at RT. Then the solvent was removed under reduced pressure and the residue was taken-up in 5 ml 5 M HCl. The acid precipitated as a brown solid and was dried under reduced pressure. Yield: 280 mg

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358268B2
Source datasetuspto-grants-2008_04
ORD IDord-0d555b500bd549179d8c67a5a5a922dc
Source noteuspto-grants-2008_04