1,4-Dioxane hydrochloride → (R)-3-Fluoro-5,11-dihydro-5-[1-(4-methoxyphenethyl)piperidin-2-yl-methyl]dibenzo[b,e][1,4]oxazepine hydrochloride
Reaktionsgleichung
[ClH:1].O1CCOCC1.[F:8][C:9]1[CH:10]=[CH:11][C:12]2[CH2:18][O:17][C:16]3[CH:19]=[CH:20][CH:21]=[CH:22][C:15]=3[N:14]([CH2:23][C@H:24]3[CH2:29][CH2:28][CH2:27][CH2:26][N:25]3[CH2:30][CH2:31][C:32]3[CH:37]=[CH:36][C:35]([O:38][CH3:39])=[CH:34][CH:33]=3)[C:13]=2[CH:40]=1>ClCCl>[ClH:1].[F:8][C:9]1[CH:10]=[CH:11][C:12]2[CH2:18][O:17][C:16]3[CH:19]=[CH:20][CH:21]=[CH:22][C:15]=3[N:14]([CH2:23][C@H:24]3[CH2:29][CH2:28][CH2:27][CH2:26][N:25]3[CH2:30][CH2:31][C:32]3[CH:37]=[CH:36][C:35]([O:38][CH3:39])=[CH:34][CH:33]=3)[C:13]=2[CH:40]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
0.3 ml of 4 M hydrogen chloride/dioxane was added to a solution of (R)-3-fluoro-5,11-dihydro-5-[1-(4-methoxyphenethyl)piperidin-2-yl-methyl]dibenzo[b,e][1,4]oxazepine (300 mg, 0.7 mmol) in dichloromethane (5 ml), and they were stirred together for 30 minutes. The solvent was evaporated under reduced pressure. The obtained residue was solidified with a mixed solvent of hexane and ethyl acetate. The solid thus precipitated was taken by the filtration to obtain the title compound in the form of a brown solid (257 mg, 79%).
Aufarbeitung
- customThe solvent was evaporated under reduced pressure
- customThe solid thus precipitated
- filtrationwas taken by the filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-d26b0276299a41a8a3212b3cc4d7f9a9
- Quelldatensatz
- uspto-grants-2008_01
- Patentnummer
- US07320973B2
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