HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromoaniline → N-(4-Bromophenyl)-4-[(propane-2-sulfonyl)amino]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-[(Propane-2-sulfonyl)amino]benzoyl chloride | HCID 13489981 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Bromophenyl)-4-[(propane-2-sulfonyl)amino]benzamide | HCID 13489982 | 52.7% |
Reaction Steps
A mixture of 250 mg of 4-isopropanesulfonamidobenzoylchloride 1, 181 mg of 4-bromoaniline 2, 106 mg of triethylamine, and 5 ml of methylene chloride is stirred at room temperature for 5 minutes. The reaction mixture is neutralized with a sodium bicarbonate solution, and extracted with methylene chloride. The organic layer is concentrated under reduced pressure, and the residue is chromatographed on a column of silica-gel. The eluate with 3% methanolmethylene chloride is concentrated, and the residue is crystallized from ethyl acetate-isopropyl ether. The crude resulting crystals are recrystallized from ethyl acetateisopropyl ether to give 200 mg of 4'-bromo-4-isopropanesulfonamidobenzanilide 3 as pure specimen, m.p. 213°-214° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04595780 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-b2d4a1026a424abfac07f803ca26f855 |
| Source note | uspto-grants-1986_06 |