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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510446Generated: November 4, 2026

Dimethyl Sulfoxide → HCID 67121130, compound

https://huagongshe.com/reaction/1510446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67121143HCID 67121143—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67121130HCID 6712113018.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of oxalyl chloride (30 μL, 0.34 mmol) in dichloromethane (1 mL) was cooled to −78° C. A solution of dimethylsulfoxide (48 μL, 0.675 mmol) in dichloromethane (0.5 mL) was added drop wise and the mixture was stirred for 5 minutes at −78° C. A solution of 4-chloro-5-(4-fluorophenyl)-N-(3-hydroxycyclohexyl)isoxazole-3-carboxamide (104 mg, 0.307 mmol) in tetrahydrofuran (3 mL) and (0.5 mL) dichloromethane was added over 5 minutes and the reaction mixture was to stirred for 15 minutes at −78° C. Triethylamine (0.215 mL, 1.53 mmol) was added and the reaction was stirred for 10 minutes at −78° C., then allowed to warm to room temperature and stir for an additional 20 minutes. Water was added and the mixture was extracted three times with dichloromethane. The combined organic extracts were dried over MgSO4, filtered, concentrated in vacuo, and purified by silica gel chromatography, eluting with 2% methanol in dichloromethane to give the title compound (19.7 mg, 0.058 mmol). MS (ESI) m/z (M+H+): 337.2/339.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211927B2
Source datasetuspto-grants-2012_07
ORD IDord-11c84090be18484bb925bc6682add1ce
Source noteuspto-grants-2012_07