반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([C:12]2[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][CH:13]=2)[CH:3]=1.[CH3:19][NH:20][C:21](=[O:28])[CH:22]1[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1.C1(O)C=CC=CC=1>O>[Cl:18][C:15]1[CH:16]=[CH:17][C:12]([C:4]2[CH:3]=[C:2]([N:25]3[CH2:26][CH2:27][CH:22]([C:21]([NH:20][CH3:19])=[O:28])[CH2:23][CH2:24]3)[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[N:5]=2)=[CH:13][CH:14]=1참가 물질
5
반응 조건
- 온도
- 160 °C
실험 절차
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.
후처리
- temperatureIt was then cooled
- customCrystallization
- temperaturewarming
- additionthe addition of a small amount of ethanol
- customThe solid was collected
- washwashed with ether
- customto give 7.0 g of crude product
- customRecrystallization from 150 ml of butanol
출처 및 근거
- ORD 기록
- ord-b64d404922d84ae8bf28e9b2f6fc0032
- 출처 데이터셋
- uspto-grants-1985_12
- 특허 번호
- US04560692
연결된 노트
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