HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoroaniline → trans-4-(4-Cyano-3-trifluoromethylphenyl)-N-(4-fluorophenyl)-2,5-dimethylpiperazine-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Sulfamide | HCID 82267 | — |
| Reactant | trans-4-(2,5-Dimethylpiperazin-1-yl)-2-trifluoromethylbenzonitrile | HCID 11391932 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | trans-4-(4-Cyano-3-trifluoromethylphenyl)-N-(4-fluorophenyl)-2,5-dimethylpiperazine-1-sulfonamide | HCID 69108864 | — |
Reaction Steps
A 1.21 g portion of trans-4-(2,5-dimethylpiperazin-1-yl)-2-trifluoromethylbenzonitrile synthesized in Reference Example 1-1 and 2.05 g of sulfamide were heated under reflux for 1.5 hours in 15 ml of pyridine. Next, this was mixed with 4.05 ml of 4-fluoroaniline and again heated under reflux for 4 hours. After evaporation of the solvent, the residue was purified by a silica gel column chromatography to obtain 701 mg of the title compound from toluene-ethyl acetate eluate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06673799B1 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-50d8bb59c75a49fe9182e1b8d5d09c23 |
| Source note | uspto-grants-2004_01 |