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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586610Generated: November 4, 2026

Methanesulfonic Acid → HCID 15097348, compound

https://huagongshe.com/reaction/1586610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantTriethylamineHCID 8471—
Reactant2-Furancarbonyl chlorideHCID 68242—
ReactantHCID 19758586HCID 19758586—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 15097348HCID 1509734880.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

6.1 g of 2-furancarboxylic acid chloride and 0.1 g of 4-dimethylaminopyridine are added to a suspension of 10.1 g of 1-(3-sulfamoylphenyl)-3,3-dimethylurea in 60 ml of acetonitrile. 9.5 g of triethylamine are added dropwise to that mixture at room temperature. The reaction mixture is stirred for 15 hours at room temperature and for one hour at 60° C. After the mixture has cooled, 4.5 g of methanesulfonic acid are added dropwise thereto and the mixture is taken up in 1 liter of water. The oil that separates out crystallises after a short time. The crystals are separated off, washed with methanol and dried, yielding 11.3 g of 1-[3-(N-2-furylcarbonylsulfamoyl)-phenyl]-3,3-dimethylurea, m.p. 216°-217° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215570
Source datasetuspto-grants-1993_06
ORD IDord-6f6b0d971a4742a886da5839a070fbc3
Source noteuspto-grants-1993_06