참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenol | HCID 996 | — |
| 반응물 | N-methylpiperidine-4-carboxamide | HCID 2760460 | — |
| 반응물 | 4-Chloro-2-(4-chlorophenyl)quinoline | HCID 11219546 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | HCID 13603913 | HCID 13603913 | 57.7% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04560692 |
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| 출처 데이터셋 | uspto-grants-1985_12 |
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| ORD ID | ord-b64d404922d84ae8bf28e9b2f6fc0032 |
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| 출처 메모 | uspto-grants-1985_12 |
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