HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21314878, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | HCID 21314846 | HCID 21314846 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21314878 | HCID 21314878 | — |
Reaction Steps
To a mixture of [[4-[(7-trifluoromethyl-4-quinolinyl)amino]phenyl]sulfonyl]piperazine (prepared as in Example 9, part D) and triethylamine, in dimethyl formamide, is added dropwise an equimolar quantity of dimethylsulfamoyl chloride. The reaction mixture is stirred at room temperature for 15 to 25 hours and is then partitioned with methylene chloride-aqueous sodium carbonate. The organic phase is dried over sodium sulfate and is concentrated and purified by conventional methods to give 1-(dimethylaminosulfonyl)-4-[[4-[[7-(trifluoromethyl)-4-quinolinyl]amino]phenyl]sulfonyl]piperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04159331 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-00dcaf8ae5324997b1fc1bc27cf10e6a |
| Source note | uspto-grants-1979_06 |