Hydrochloric Acid → HCID 86754624, Verbindung
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([C:8]2(O)[CH2:17][CH2:16][C@@H:15]3[C@:10]([C:20]4[CH:25]=[CH:24][CH:23]=[C:22]([O:26][CH3:27])[CH:21]=4)([CH2:11][CH2:12][N:13]([CH2:18][CH3:19])[CH2:14]3)[CH2:9]2)[CH:5]=[CH:6][CH:7]=1.Cl>>[NH4+:13].[OH-:26].[Br:1][C:2]1[CH:3]=[C:4]([C:8]2[CH2:9][C@:10]3([C:20]4[CH:25]=[CH:24][CH:23]=[C:22]([O:26][CH3:27])[CH:21]=4)[C@@H:15]([CH2:16][CH:17]=2)[CH2:14][N:13]([CH2:18][CH3:19])[CH2:12][CH2:11]3)[CH:5]=[CH:6][CH:7]=1Komponenten
4
Versuchsvorschrift
The reaction was conducted as described in Example 2, using 0.44 g (0.99 mmol) of (±)-trans-6-(3-bromophenyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinol and 15 ml of 37% HCl. The crude reaction mixture was purified by flash chromatography, eluting with a mixture CH2Cl2 /MeOH/conc. NH4OH 98:2:0.4 respectively, yielding 0.25 g of the title compound.
Aufarbeitung
- customThe crude reaction mixture
- customwas purified by flash chromatography
- washeluting with a mixture CH2Cl2 /MeOH/conc
Quellen und Nachweise
- ORD-Eintrag
- ord-637aa65fceed4eb7826e910f57122ee6
- Quelldatensatz
- uspto-grants-1999_10
- Patentnummer
- US05968949
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