Iodoethane → 2-[3-(6-Chloro-2-methyl-1-pyridin-3-yl-1H-indol-3-ylsulfanyl)-phenyl]butyric acid ethyl ester
Reaktionsgleichung
[CH2:1]([O:3][C:4](=[O:30])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([S:12][C:13]2[C:21]3[C:16](=[CH:17][C:18]([Cl:22])=[CH:19][CH:20]=3)[N:15]([C:23]3[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=3)[C:14]=2[CH3:29])[CH:7]=1)[CH3:2].I[CH2:32][CH3:33]>>[CH2:1]([O:3][C:4](=[O:30])[CH:5]([C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([S:12][C:13]2[C:21]3[C:16](=[CH:17][C:18]([Cl:22])=[CH:19][CH:20]=3)[N:15]([C:23]3[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=3)[C:14]=2[CH3:29])[CH:7]=1)[CH2:32][CH3:33])[CH3:2]Komponenten
3
Versuchsvorschrift
Prepared according to the procedure described in Example 108, step 1, using the following starting materials: [3-(6-Chloro-2-methyl-1-pyridin-3-yl-1H-indol-3-ylsulfanyl)-phenyl]-acetic acid ethyl ester and iodoethane.
Aufarbeitung
- customPrepared