HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Difluoromethoxy)aniline → N-[3-(Difluoromethoxy)phenyl]-4-methyl-3-[4-(2,2,2-trifluoroacetyl)-1-piperazinyl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Difluoromethoxy)aniline | HCID 2774110 | — |
| Reactant | HCID 59563966 | HCID 59563966 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[3-(Difluoromethoxy)phenyl]-4-methyl-3-[4-(2,2,2-trifluoroacetyl)-1-piperazinyl]benzenesulfonamide | HCID 59563972 | 47.3% |
Reaction Steps
0.429 g of 3-(difluoromethoxy)-aniline (2.7 mmol) were dissolved in 5 mL of pyridine. 1 g of 4-methyl-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonylchloride (2.7 mmol) were added slowly at room temperature. After stirring for 16 h at room temperature, the reaction mixture was evaporated several times after addition of toluene. The residue was dissolved in dichloromethane and washed several times with 5% aqueous ammonium chloride. The organic phase was then washed with saturated aqueous sodium chloride, dried over sodium sulphate, filtered, and the solvent evaporated. The crude product was purified via silica gel chromatography using dichloromethane/methanol (0-5%) to yield 0.63 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076326B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-6a2ff749fa604e1abaa2b5f9f2045ebc |
| Source note | uspto-grants-2011_12 |