HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-bromo-1-(2-cyanophenylsulfonyl)-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Cyanobenzenesulfonyl Chloride | HCID 522347 | — |
| Reactant | HCID 178419483 | HCID 178419483 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromo-1-(2-cyanophenylsulfonyl)-1H-indazole | HCID 118264732 | 97.4% |
Reaction Steps
To a solution of 3-bromo-1H-indazole (200 mg, 1.02 mmol) in 2 ml CH2Cl2 was added triethylamine (308 mg, 3.05 mmol) and 2-cyanobenzene-1-sulfonyl chloride (205 mg, 1.02 mmol). The reaction mixture was stirred overnight at room temperature. After completion the reaction mixture was concentrated under reduced pressure and the product was purified on SiO2 using 0% to 50% ethyl acetate in heptane as the eluent to give 3-bromo-1-(2-cyanophenylsulfonyl)-1H-indazole (360 mg) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09095583B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-8294b3517441414c81b59b42493ccab1 |
| Source note | uspto-grants-2015_08 |