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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904797Generated: October 31, 2026

Hydrochloric Acid → 1-(4-Methanesulfonylaminophenyl)-3-azabicyclo[3.1.0]hexane-2,4dione

https://huagongshe.com/reaction/1904797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-(4-Aminophenyl)-3-azabicyclo[3.1.0]hexane-2,4-dioneHCID 14068934—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product1-(4-Methanesulfonylaminophenyl)-3-azabicyclo[3.1.0]hexane-2,4dioneHCID 20038048—

Reaction Steps

A solution of 1.2 ml of methanesulfonyl chloride in 10 ml of methylene chloride is stirred dropwise at room temperature into a mixture of 3 g of 1-(4-aminophenyl)-3-azabicyclo[3.1.0]hexane-2,4-dione, 90 mg of dimethylaminopyridine and 37 ml of pyridine. After it has been stirred for 16 hours, the reaction mixture is freed from solvent in vacuo. The residue is dissolved in 100 ml of water and the solution is adjusted to pH 1 with hydrochloric acid. After further stirring, the crystals are isolated by filtration and recrystallised from methanol. The title compound is obtained in the form of whitish orange crystals with a melting point of 208°-209° C. and with Rf=0.32 on thin-layer silica gel plates in the system methylene chloride/methanol (10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839379
Source datasetuspto-grants-1989_06
ORD IDord-dde90decdc3649e6ade0b9a2e1d3ef3e
Source noteuspto-grants-1989_06