Methyl iodide → N-(2-{6-Chloro-3-[4-(2-fluoro-phenyl)-piperazine-1-carbonyl]-indol-1-yl}-ethyl)-N-methyl-acetamide
반응식
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:18]([N:20]3[CH2:25][CH2:24][N:23]([C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=4[F:32])[CH2:22][CH2:21]3)=[O:19])=[CH:7][N:8]2[CH2:11][CH2:12]CS(N)(=O)=O)=[CH:4][CH:3]=1.[H-].[Na+].CI>CN(C=O)C>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:18]([N:20]3[CH2:25][CH2:24][N:23]([C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=4[F:32])[CH2:22][CH2:21]3)=[O:19])=[CH:7][N:8]2[CH2:11][CH2:12][N:20]([CH3:21])[C:18](=[O:19])[CH3:6])=[CH:4][CH:3]=1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
N-(2-{6-Chloro-3-[4-(2-fluoro-phenyl)-piperazine-1-carbonyl]-indol-1-yl}-ethyl-methanesulfonamide (preparation described herein), was treated with NaH (1.05 eq), MeI (1.05 eq) in dry DMF under argon at RT for 2 h to give after purification by prep. HPLC the title compound.
후처리
- customto give
- customafter purification by prep
출처 및 근거
- ORD 기록
- ord-e0a87949adfe4d31a4ed72f0a0a5d790
- 출처 데이터셋
- uspto-grants-2010_08
- 특허 번호
- US07781436B2
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