반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH2:11])(=[O:10])=[O:9])=[CH:4][C:3]=1[N+]([O-])=O.[O:15]1[CH2:20][CH2:19][CH:18]([CH2:21][NH2:22])[CH2:17][CH2:16]1.[ClH:23].Cl.CN1CCN(N)CC1.CCN(C(C)C)C(C)C.CN(C)CCN(C)C>>[Cl:23][C:3]1[CH:4]=[C:5]([S:8]([NH2:11])(=[O:10])=[O:9])[CH:6]=[CH:7][C:2]=1[NH:22][CH2:21][CH:18]1[CH2:19][CH2:20][O:15][CH2:16][CH2:17]1참가 물질
6
반응물 5
생성물 1
실험 절차
The title compound was prepared by substituting 4-fluoro-3-chlorobenzenesulfonamide for 4-chloro-3-nitrobenzenesulfonamide, (tetrahydro-2H-pyran-4-yl)methanamine for 4-methylpiperazin-1-amine dihydrochloride and Hunig's base for N1, N1,N2,N2-tetramethylethane-1,2-diamine in EXAMPLE 6A.
출처 및 근거
- ORD 기록
- ord-e4f76a412a6b4a3c88c2d7fa1cabee2f
- 출처 데이터셋
- uspto-grants-2015_05
- 특허 번호
- US09034875B2
연결된 노트
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