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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465280Generated: October 29, 2026

phenyl N-[(N-dimethylsulfamoyl-N-methylamino)sulfonyl]carbamate → 1-[(N-dimethylsulfamoyl-N-methylamino)sulfonylcarbamoyl]-3-methyl-5-(2-thienyl)-2-pyrazoline

https://huagongshe.com/reaction/465280

Reaction equation

Participants

RoleNameHCIDCharge
Reactantphenyl N-[(N-dimethylsulfamoyl-N-methylamino)sulfonyl]carbamateHCID 19873528—
Reactant3-Methyl-5-(2-thienyl)-2-pyrazolineHCID 19873529—
SolventBenzeneHCID 241—
Product1-[(N-dimethylsulfamoyl-N-methylamino)sulfonylcarbamoyl]-3-methyl-5-(2-thienyl)-2-pyrazolineHCID 1987353076.7%

Reaction Steps

A mixture comprising 1.69 g (5.0 mmol) of phenyl N-[(N-dimethylsulfamoyl-N-methylamino)sulfonyl]carbamate, 0.58 g (3.5 mmol) of 3-methyl-5-(2-thienyl)-2-pyrazoline and 10 ml of dry benzene, was refluxed for 10 minutes. The mixture was left to cool, and then benzene was distilled off under reduced pressure. The obtained residue was washed with n-hexane. Then, the residue was stirred together with diethyl ether. The precipitated crystalline product was isolated by suction filtration and then washed with diethyl ether to obtain 1.1 g of the desired 1-[(N-dimethylsulfamoyl-N-methylamino)sulfonylcarbamoyl]-3-methyl-5-(2-thienyl)-2-pyrazoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05152824
Source datasetuspto-grants-1992_10
ORD IDord-7852223a462f4d96b9c43a3b7ce1ed21
Source noteuspto-grants-1992_10