HCID 18186376, Verbindung → HCID 18186382, Verbindung
Reaktionsgleichung
[N:1]1([C:7]2[CH:38]=[CH:37][C:10]([CH2:11][CH:12]3[C:21]4[C:16](=[CH:17][C:18]([O:22]CC5C=CC=CC=5)=[CH:19][CH:20]=4)[CH2:15][CH2:14][N:13]3[C:30]3[CH:35]=[CH:34][C:33]([F:36])=[CH:32][CH:31]=3)=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1>[Pd]>[N:1]1([C:7]2[CH:38]=[CH:37][C:10]([CH2:11][CH:12]3[C:21]4[C:16](=[CH:17][C:18]([OH:22])=[CH:19][CH:20]=4)[CH2:15][CH2:14][N:13]3[C:30]3[CH:31]=[CH:32][C:33]([F:36])=[CH:34][CH:35]=3)=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Komponenten
3
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1-{4-(N-Piperidyl)benzyl}-2-(4-fluorophenyl}-6-phenylmethoxy-1,2,3,4-tetrahydroisoquinoline (0.25 g, 0.49 mmol) was treated with H2 in 10% Pd/C as described in Example 14. D to yield 1-{4-(N-piperidyl)benzyl}-2-(4-fluorophenyl}-1,2,3,4-tetrahydroisoquinoline-6-ol. Treatment of the free base with conc. HCl in ether produces a fine white solid. The precipitate is filtered and dried under high vacuum to yield the title compound. (0.096 g, 47% yield): m.p. 177-179° C. (dec.).
Quellen und Nachweise
- ORD-Eintrag
- ord-fb690081ffd7452dafc59bb04c028873