HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(propan-2-yl)-1H-indole → HCID 58975178, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(propan-2-yl)-1H-indole | HCID 12534824 | — |
| Reactant | Water ethylacetate | HCID 22728543 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride | HCID 58975125 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58975178 | HCID 58975178 | — |
Reaction Steps
Stir a mixture of 3-isopropyl indole in dry DMF (20 ml) under N2 add potassium t-butoxide 1.0 M (1.2 ml, 1.2 mmol) dropwise. Stir the resulting solution for 30 minutes at ambient temperature. Add 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (0.360 g, 1.1 mmol) portionwise and stir the resulting mixture overnight. Pour the reaction mixture into a mixture of EtOAc—H2O. Separate the EtOAc layer, extract with H2O wash with brine and dry (MgSO4). Filter and evaporate to give the crude product. Chromatograph on the ISCO eluting with hexane-EtOAc to give a white solid (0.150 g). Mass spectrum (m/e) (M+H) 451.1492; found 451.1488.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595339B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-6e6db808672844b2aa9b6035559abfb4 |
| Source note | uspto-grants-2009_09 |