반응식
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([NH2:8])[CH2:4][CH2:3]1.Cl[C:10]1[N:11]([C:30](=[O:32])[CH3:31])[CH2:12][C:13]2[N:19]=[C:18]([Cl:20])[N:17]=[C:16]([NH:21][C:22]3[CH:27]=[CH:26][C:25]([F:28])=[C:24]([Cl:29])[CH:23]=3)[C:14]=2[N:15]=1.C1COCC1.C(N(CC)CC)C>O>[Cl:20][C:18]1[N:17]=[C:16]([NH:21][C:22]2[CH:27]=[CH:26][C:25]([F:28])=[C:24]([Cl:29])[CH:23]=2)[C:14]2[N:15]=[C:10]([NH:8][CH:5]3[CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]3)[N:11]([C:30](=[O:32])[CH3:31])[CH2:12][C:13]=2[N:19]=1참가 물질
6
반응 조건
- 온도
- 50 °C
실험 절차
47.2 g (0.413 mol) of 1-methyl-4-aminopiperidine is added dropwise at ambient temperature to a mixture of 123.3 g (0.317 mol) of (3), 740 ml of THF and 61.7 ml (0.445 mol) of triethylamine. The mixture is stirred for 30 min at 50° C. It is left to cool to 40° C., 1480 ml of water are added and the mixture is then stirred for 90 minutes at 10° C. The product that crystallises out is filtered off, washed with 150 ml of water and dried in vacuo at 60° C. The product is dissolved in 1150 ml of ethyl acetate at boiling temperature. It is cooled to 10° C., filtered and the product that crystallises out is dried at 60° C. in vacuo. Yield: 128.9 g (87.2%).
후처리
- waitIt is left
- temperatureto cool to 40° C.
- stirringthe mixture is then stirred for 90 minutes at 10° C
- customThe product that crystallises out
- filtrationis filtered off
- washwashed with 150 ml of water
- customdried in vacuo at 60° C
- dissolutionThe product is dissolved in 1150 ml of ethyl acetate
- temperatureIt is cooled to 10° C.
- filtrationfiltered
- customthe product that crystallises out
- customis dried at 60° C. in vacuo
출처 및 근거
- ORD 기록
- ord-06a7203e45974abea770c02cd055dcd5
- 출처 데이터셋
- uspto-grants-2005_02
- 특허 번호
- US06849734B2
연결된 노트
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