HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride, 3,4-dichloro- → HCID 22057976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride, 3,4-dichloro- | HCID 76403 | — |
| Reactant | HCID 22057974 | HCID 22057974 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22057976 | HCID 22057976 | 57% |
Reaction Steps
Using an analogous procedure to that described in Example 4, 3,4-dichlorobenzoyl 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 16 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 57% 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-7711a4b58b77402fa9925ea9c6d141c9 |
| Source note | uspto-grants-2006_06 |