HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Hexahydro-1-[[4-(trifluoromethyl)phenyl]sulfonyl]-1H-1,4-diazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Hexahydro-1-[[4-(trifluoromethyl)phenyl]sulfonyl]-1H-1,4-diazepine | HCID 18698051 | 95.2% |
Reaction Steps
The 1-(4-trifluoromethylphenylsulphonyl)homopiperazine was prepared as follows. 4-Trifluoromethylphenylsulphonylchloride (1.5 g) in 20 ml dichloromethane was added dropwise to 5 g homopiperazine and 1.8 ml triethylamine in 55 ml dichloromethane and left stirring overnight. Washed with water and brine, dried (MgSO4), and evaporated to give 1-(4-trifluoromethylphenylsulphonyl)homopiperazine (1.80 g) as a colourless solid; NMR (CDCl3) 1.75 (1H,br), 1.78-1.9 (2H,m), 2.9-3.0 (4H,m), 3.3-3.44 (4H,m), 7.78 (2H,d),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093718 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-1e8051e9fb714f51a407d13284e7964d |
| Source note | uspto-grants-2000_07 |