Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | N-methylpiperidine-4-carboxamide | HCID 2760460 | — |
| Reactant | 4-Chloro-2-(4-chlorophenyl)quinoline | HCID 11219546 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13603913 | HCID 13603913 | 57.7% |
Reaction Steps
A mixture of 5.1 g (21 mmole) of 4-chloro-2-(4-chlorophenyl)quinoline, prepared as in Example 1(a), 6.2 g (42 mmole) of N-methylisonipecotamide, and 10 g of phenol was stirred and heated in an oil bath at 160° C. for 3.5 hr. It was then cooled and diluted with 100 ml of water. Crystallization was induced by scratching, warming and the addition of a small amount of ethanol. The solid was collected and washed with ether to give 7.0 g of crude product. Recrystallization from 150 ml of butanol gave 4.6 g of product, mp 251°-255° dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560692 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-b64d404922d84ae8bf28e9b2f6fc0032 |
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| Source note | uspto-grants-1985_12 |
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