HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Methoxy-6-(trifluoromethyl)indoline → HCID 10837468, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Methoxy-6-(trifluoromethyl)indoline | HCID 11206713 | — |
| Reactant | HCID 18005145 | HCID 18005145 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10837468 | HCID 10837468 | 26% |
Reaction Steps
Phenyl N-[2,3-dihydro-7-(pyrid-3-yl)benzofuran-5-yl]carbamate (D65) (0.20 g, 0.00060 mole) in dry DMF (10 ml) was treated under argon with 5-methoxy-6-trifluoromethyl indoline (D11) (0.13 g, 0.00060 mole) and heated under reflux for 18 hours. The reaction was allowed to cool to ambient temperature and the solvent was removed in vacuo. The residue was dissolved in dichloromethane, washed with deionised water and 10% sodium hydroxide solution, dried (Na2SO4) and evaporated in vacuo. The resulting brown oil was purified by flash column chromatography on silica gel eluting with 2% methanol/dichloromethane, followed by recrystallisation from ethyl acetate 60.80° petroleum ether to afford the title compound (0.07 g, 26%) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06638953B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-56e7dc40820441d6a59207a31ee01d62 |
| Source note | uspto-grants-2003_10 |