HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-7-(trifluoromethyl)quinoline → 4-[(4-Fluorophenyl)hydroxymethyl]-1-[4-[[7-(trifluoromethyl)-4-quinolyl]amino]benzoyl]piperidine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-7-(trifluoromethyl)quinoline | HCID 67668 | — |
| Reactant | 1-(4-Aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidine | HCID 13825043 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[(4-Fluorophenyl)hydroxymethyl]-1-[4-[[7-(trifluoromethyl)-4-quinolyl]amino]benzoyl]piperidine hydrochloride | HCID 20144931 | 84.7% |
Reaction Steps
A mixture of 4-chloro-7-(trifluoromethyl)quinoline (0.32 g) and 1-(4-aminobenzoyl)-4-[(4-fluorophenyl)hydroxymethyl]piperidine (0.45 g) in dry ethanol (10 ml) was stirred under reflux for 4 hours and concentrated to dryness in vacuo. The residue was recrystallized from a mixture of ethyl acetate and isopropanol to give 4-[(4-fluorophenyl)hydroxymethyl]-1-[4-[[7-(trifluoromethyl)-4-quinolyl]amino]benzoyl]piperidine hydrochloride (0.65 g) as pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04735952 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-2bd6b18266c1413c914439e2c3b555d6 |
| Source note | uspto-grants-1988_04 |