HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 56966718, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-Fluorobenzenesulfonyl Chloride | HCID 2734258 | — |
| Reactant | HCID 67290769 | HCID 67290769 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 56966718 | HCID 56966718 | — |
Reaction Steps
To a stirred solution of 2-(6-chloro-4,4-dimethyl-1,2,3,4-tetrahydroquinolin-2-yl)aniline (100 mg, 0.35 mmol) in dichloromethane (5 mL) was added pyridine (0.6 mL) and 3-fluorobenzenesulfonyl chloride (68 mg, 0.35 mmol) at ice-bath. The reaction mixture was stirred at room temperature overnight. The reaction mixture was washed with water. The aqueous layer was extracted with dichloromethane. The combined organic layer was washed by brine, dried over anhydrous sodium sulfate, concentrated in vacuo. The residue was purified by HPLC to give N-[2-(6-chloro-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-3-fluoro-benzenesulfonamide. LC/MS m/e obsd. (ESI−) [(M−H)−] 443.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546427B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-5d181c61d8504a75ab33edfd1aef85fa |
| Source note | uspto-grants-2013_10 |