Reaktionsgleichung
[C:1]([O:5][C:6](=[O:29])[NH:7][C:8]([CH3:28])([CH3:27])[CH2:9][C:10]1[C:18]2[C:13](=[C:14]([CH2:19]S(C(F)(F)F)(=O)=O)[CH:15]=[CH:16][CH:17]=2)[NH:12][CH:11]=1)([CH3:4])([CH3:3])[CH3:2].[C:30]([C:32]1[CH:39]=[CH:38][C:35]([CH:36]=C)=[CH:34][CH:33]=1)#[N:31]>>[C:1]([O:5][C:6](=[O:29])[NH:7][C:8]([CH3:28])([CH3:27])[CH2:9][C:10]1[C:18]2[C:13](=[C:14]([CH:19]=[CH:36][C:35]3[CH:38]=[CH:39][C:32]([C:30]#[N:31])=[CH:33][CH:34]=3)[CH:15]=[CH:16][CH:17]=2)[NH:12][CH:11]=1)([CH3:4])([CH3:3])[CH3:2]Komponenten
3
Versuchsvorschrift
(2-{7-[2-(4-Cyano-phenyl)-vinyl]-1H-indol-3-yl}-1,1-dimethyl-ethyl)-carbamic acid tert-butyl ester is prepared from [1,1-dimethyl-2-(7-trifluoromethanesulfonylmethyl-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl ester and 4-cyanostyrene as described for the preparation of Amine 23 (93%). FDMS m/e=315.2 (M++1).
Quellen und Nachweise
- ORD-Eintrag
- ord-dae3860bb7c74f11a4d843cfd6f15f97
- Quelldatensatz
- uspto-grants-2007_04
- Patentnummer
- US07208505B2
Verknüpfte Notizen
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