HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-[2-(4-Chlorophenyl)-4-quinolinyl]-4-piperidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Piperidinecarboxamide | HCID 3772 | — |
| Reactant | 4-Chloro-2-(4-chlorophenyl)quinoline | HCID 11219546 | — |
| Solvent | Phenol | HCID 996 | — |
| Product | 1-[2-(4-Chlorophenyl)-4-quinolinyl]-4-piperidinecarboxamide | HCID 13603914 | — |
Reaction Steps
In a manner analogous to that of Example 6, 4-chloro-2-(4-chlorophenyl)quinoline was reacted with isonipecotamide in phenol at 170° C., yielding the named compound, mp. 245°-247° dec., from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04560692 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-dfb63a18cc624a76ac643089f08d8317 |
| Source note | uspto-grants-1985_12 |