반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:13]([CH2:20]Cl)=[CH:12]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[NH:22]1[CH2:28][CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1>>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:13]([CH2:20][N:22]3[CH2:28][CH2:27][CH2:26][NH:25][CH2:24][CH2:23]3)=[CH:12]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1참가 물질
3
실험 절차
Using essentially the same procedure as described in example 127, 1-(4-methylbenzenesulfonyl)-3-chloromethyl-1H-indole was reacted with homopiperazine to obtain the above derivative.
후처리
- customto obtain the above derivative
출처 및 근거
- ORD 기록
- ord-adecabc3be0b45bc92784c23edc61bfb
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07875605B2
연결된 노트
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