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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183796Generated: November 2, 2026

Benzenesulfonic Acid → 4-Carbamoylimidazolium 5-olate

https://huagongshe.com/reaction/1183796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic AcidHCID 7371—
ReactantTrimethyl orthoformateHCID 9005—
Reactant2-AminopropanediamideHCID 96457—
ReactantHydroxybenzenesulfonic acidHCID 15619088—
SolventEthanolHCID 702—
ProductBenzenesulfonic AcidHCID 7371—
Product4-Carbamoylimidazolium 5-olateHCID 12434382%

Reaction Steps

Into a suspension of benzenesulfonic acid salt of 2-aminomalonamide [4] (1.20 g; 4.37 mmol) prepared above and benzenesulfonic acid monohydrate (81 mg; 0.46 mmol) in dry ethanol (100 ml) was added trimethyl orthoformate (1.9 ml; 17.4 mmol), and was refluxed for 2 hours under an argon atmosphere. The resulting white suspension was stirred overnight at room temperature and the precipitates were collected by filtration to give colorless benzenesulfonic acid salt of SM-108 (1.02 g; 3.58 mmol; yield 82%), which was identical with that obtained in Example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664405B2
Source datasetuspto-grants-2014_03
ORD IDord-89a35ac613174ff7ba10406a8b3ea7f5
Source noteuspto-grants-2014_03