HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-4-(2-nitro-4-(trifluoromethyl)phenylsulfonyl)piperazine → 2-(4-Methylpiperazin-1-ylsulfonyl)-5-(trifluoromethyl)benzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-4-(2-nitro-4-(trifluoromethyl)phenylsulfonyl)piperazine | HCID 68463407 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Methylpiperazin-1-ylsulfonyl)-5-(trifluoromethyl)benzenamine | HCID 59427881 | — |
Reaction Steps
1-methyl-4-(2-nitro-4-(trifluoromethyl)phenylsulfonyl)piperazine was dissolved in EtOH (20 mL) and the solution was purged with argon. Pd/C (365 mg, 0.34 mmol, 10%) was added to the solution, which was stirred for 3 days in an atmosphere of hydrogen gas. The mixture was again purged with argon, filtered through Celite and concentrated under reduced pressure to afford 2-(4-methylpiperazin-1-ylsulfonyl)-5-(trifluoromethyl)benzenamine. MS m/z=324 [M+H]+. Calc'd for C12H16F3N3O2S: 323.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557996B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-093d617e8d354d178ae13bbdd8f1074a |
| Source note | uspto-grants-2013_10 |