Reaktionsgleichung
[O:1]1[C:5]2([CH2:10][CH2:9][C:8]([C:11]3[C:19]4[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=4)[NH:13][CH:12]=3)=[CH:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.[F:20]C1C=C2C(C=CN2)=CC=1>>[O:4]1[C:5]2([CH2:10][CH2:9][C:8]([C:11]3[C:19]4[C:14](=[CH:15][C:16]([F:20])=[CH:17][CH:18]=4)[NH:13][CH:12]=3)=[CH:7][CH2:6]2)[O:1][CH2:2][CH2:3]1Komponenten
3
Versuchsvorschrift
This compound was prepared in the manner described for intermediate 1a by replacing indole with 6-fluoroindole (5.14 g, 38 mmol) ) to afford 10 g (96.3%) of the title compound as a white solid: mp 196-197° C.
Aufarbeitung
- customThis compound was prepared in the manner
Quellen und Nachweise
- ORD-Eintrag
- ord-073920222edc4c1988928536db1edb8e
- Quelldatensatz
- uspto-grants-2001_11
- Patentnummer
- US06313126B1
Verknüpfte Notizen
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