HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-5-(trifluoromethyl)benzene-1-sulfonyl chloride → 3-[4-(2-Fluoro-5-trifluoromethylbenzenesulfonylamino)phenyl]-1H-indole-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-5-(trifluoromethyl)benzene-1-sulfonyl chloride | HCID 2737547 | — |
| Reactant | 3-(4-Aminophenyl)-1H-indole-2-carboxamide | HCID 57762833 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-[4-(2-Fluoro-5-trifluoromethylbenzenesulfonylamino)phenyl]-1H-indole-2-carboxamide | HCID 11619889 | — |
Reaction Steps
162 mg of 2-fluoro-5-trifluoromethylphenylsulfonyl chloride in 6 ml of pyridine are added dropwise to a solution of 100 mg of 3-(4-aminophenyl)-1H-indole-2-carboxamide (example 1) in 12 ml of pyridine at 0° C. The mixture is stirred at ambient temperature for 6 hours and then poured into 50 ml of ice-cold water, and the precipitate formed is filtered off. After purification by flash chromatography on a silica column, elution being carried out with a mixture of cyclohexane and ethyl acetate (20/80 by volume), 50 mg of 3-[4-(2-fluoro-5-trifluoromethylbenzenesulfonylamino)phenyl]-1H-indole-2-carboxamide are obtained, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566736B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-b45ca98aeefc46188696ded7fd98f9b5 |
| Source note | uspto-grants-2009_07 |