HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethyl)benzoyl chloride → HCID 22057983, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethyl)benzoyl chloride | HCID 67607 | — |
| Reactant | HCID 22057974 | HCID 22057974 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22057983 | HCID 22057983 | 52% |
Reaction Steps
Using an analogous procedure to that described in Example 4, 4-trifluoromethylbenzoyl chloride was reacted with N-(5-amino-2-methylphenyl)-quinoline-6-carboxamide in the presence of triethylamine. The reaction mixture was stirred at ambient temperature for 18 hours and then evaporated. The residue was purified by column chromatography on silica using increasingly polar mixtures of methylene chloride and methanol as eluent. There was thus obtained the title compound in 52% yield; Mass Spectrum: M+H+ 450.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060700B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-cd0c771dd6a54a6ca16a150c8ab4a1f7 |
| Source note | uspto-grants-2006_06 |