반응식
[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:27])[F:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:29][C:30]1[CH:35]=[C:34]([CH:36]=O)[CH:33]=[C:32]([Cl:38])[N:31]=1>>[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH:24][CH2:36][C:34]3[CH:33]=[C:32]([Cl:38])[N:31]=[C:30]([Cl:29])[CH:35]=3)[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:26])[F:27])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
3
실험 절차
This compound was prepared according to the procedure of example 66, substituting 3-(3-benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine and 2,6-dichloro-pyridine-4-carbaldehyde. MS (ESI) m/z 535.
후처리
- customThis compound was prepared
출처 및 근거
- ORD 기록
- ord-a7405565a73a47f3a1346794c818fe03
- 출처 데이터셋
- uspto-grants-2009_08
- 특허 번호
- US07576215B2
연결된 노트
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