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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076920Generated: November 1, 2026

Dimethyl Sulfoxide → 4-(Furan-2-yl)-N-(2-oxocyclohexyl)-1,3-thiazole-2-carboxamide

https://huagongshe.com/reaction/2076920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(Furan-2-yl)-N-(2-hydroxycyclohexyl)-1,3-thiazole-2-carboxamideHCID 67118892—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-(Furan-2-yl)-N-(2-oxocyclohexyl)-1,3-thiazole-2-carboxamideHCID 6711853983%

Reaction Conditions

Temperature-60 °C

Reaction Steps

Oxalyl chloride (0.776 mL, 1.55 mol) and dimethyl sulfoxide (0.240 mL, 3.38 mmol) were dissolved in dichloromethane (3 mL), and the mixture was stirred at −60° C. for 10 minutes. To the solution was added 4-(2-furyl)-N-(2-hydroxycyclohexyl)thiazole-2-carboxamide (413 mg, 1.41 mmol) obtained in Step 1 and the mixture was stirred for 15 minutes. Triethylamine (0.983 mL, 7.05 mmol) was added to the mixture, and the mixture was stirred at room temperature for 10 minutes, then water and ethyl acetate were added thereto and the mixture was extracted. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was then evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give 4-(2-furyl)-N-(2-oxocyclohexyl)thiazole-2-carboxamide (339 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928098B2
Source datasetuspto-grants-2011_04
ORD IDord-49a867885bce44ba88bd17531c4b521f
Source noteuspto-grants-2011_04