반응식
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[N:12]2[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([N+]([O-])=O)[CH:21]=3)[CH2:14][CH2:13]2)[N:3]=1.CC1C=CC2C(=CC=CC=2N2CCNCC2)N=1.CS(OCCC1C=CC=C([Br:59])C=1)(=O)=O>>[Br:59][C:22]1[CH:21]=[C:20]([CH2:19][CH2:18][N:15]2[CH2:14][CH2:13][N:12]([C:8]3[CH:7]=[CH:6][CH:5]=[C:4]4[C:9]=3[CH:10]=[CH:11][C:2]([CH3:1])=[N:3]4)[CH2:17][CH2:16]2)[CH:25]=[CH:24][CH:23]=1참가 물질
4
실험 절차
The title compound was prepared in 56% yield using a similar procedure to description D5 starting from 2-methyl-5-(1-piperazinyl)quinoline (D3) and 2-(3-bromophenyl)ethyl methanesulfonate (D13).
출처 및 근거
- ORD 기록
- ord-5db34a42240e480c884c3e96136bf5ea
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07732600B2
연결된 노트
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