HuagongsheHuagongshe Chemistry Print Report · For research reference only
phenyl N-[(N-dimethylsulfamoyl-N-methylamino)sulfonyl]carbamate → 1-[(N-dimethylsulfamoyl-N-methylamino)sulfonylcarbamoyl]-3-methyl-5-(2-thienyl)-2-pyrazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | phenyl N-[(N-dimethylsulfamoyl-N-methylamino)sulfonyl]carbamate | HCID 19873528 | — |
| Reactant | 3-Methyl-5-(2-thienyl)-2-pyrazoline | HCID 19873529 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-[(N-dimethylsulfamoyl-N-methylamino)sulfonylcarbamoyl]-3-methyl-5-(2-thienyl)-2-pyrazoline | HCID 19873530 | 76.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05152824 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-7852223a462f4d96b9c43a3b7ce1ed21 |
| Source note | uspto-grants-1992_10 |