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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106972Generated: October 28, 2026

Methanesulfonic Acid → HCID 53932011, compound

https://huagongshe.com/reaction/2106972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 22104197HCID 22104197—
ReactantHCID 23046967HCID 23046967—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 53932011HCID 5393201195%

Reaction Steps

2.4 g (0.008 mol) of 2-methoxycarbonyl-4-phenylthiophen-3-ylsulfonamide, 2.2 g of N-(4,6-dimethoxypyrimidin-2-yl)phenylcarbamate, 1.2 g of 1,8-diazabicyclo[5.4.0]undec-7-ene and 30 ml of acetonitrile are stirred for 16 hours at room temperature. The reaction mixture is then poured into a mixture of ice and water and acidified with methanesulfonic acid. The resultant precipitate is filtered, washed with water and dried, affording 3.4 g (95%) of N-(2-methoxycarbonyl-4-phenylthiophen-3-ylsulfonyl)-N'-(4,6-dimethoxypyrimidin-2-yl)urea with a melting point of 225°-227° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04932997
Source datasetuspto-grants-1990_06
ORD IDord-999600579af4437c9ef50d6959fe0c86
Source noteuspto-grants-1990_06