HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-bromo-1-(2-(trifluoromethyl)phenylsulfonyl)-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Trifluoromethylbenzenesulphonyl chloride | HCID 136616 | — |
| Reactant | HCID 178419483 | HCID 178419483 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromo-1-(2-(trifluoromethyl)phenylsulfonyl)-1H-indazole | HCID 68159272 | 86.9% |
Reaction Steps
To a suspension of 3-bromoindazole (500 mg, 2.54 mmol) in 8 ml CH2Cl2 was added triethyl amine (1.06 ml, 7.61 mmol) at room temperature. To this yellow solution was added 2-(trifluoromethyl)benzenesulfonyl chloride (0.392 ml, 2.54 mmol) and the reaction mixture was stirred for 3 h at room temperature. The reaction mixture was concentrated under reduced pressure and the residue was purified on SiO2 using 5% to 20% ethyl acetate in heptane to give 3-bromo-1-(2-(trifluoromethyl)phenylsulfonyl)-1H-indazole (894 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09095583B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-9bb6984f92b749809f85999c622bd14c |
| Source note | uspto-grants-2015_08 |