Hydrochloric Acid → HCID 68547925, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([C@:9]23[CH2:15][C@@:14]2([CH2:16][O:17][CH3:18])[CH2:13][N:12]([CH3:19])[CH2:11][CH2:10]3)[CH:5]=[CH:6][C:7]=1[Cl:8].Cl>C(OCC)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([C@:9]23[CH2:15][C@@:14]2([CH2:16][O:17][CH3:18])[CH2:13][N:12]([CH3:19])[CH2:11][CH2:10]3)[CH:5]=[CH:6][C:7]=1[Cl:8]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
(1S,6R)-6-(3,4-dichlorophenyl)-3-methyl-1-[(methyloxy)methyl]-3-azabicyclo[4.1.0]heptane (E12, 16 mg) was treated with hydrochloric acid 1.0M in diethyl ether (0.064 mL). 0.5 mL of diethyl ether were added and a colourless solid formed. Organic phase was removed after decantation of the solid. Colourless solid obtained as a 5:1 mixture of isomers due protonation on the nitrogen atom (16 mg).
Aufarbeitung
- customa colourless solid formed
- customOrganic phase was removed after decantation of the solid
- customColourless solid obtained as a 5:1 mixture of isomers due protonation on the nitrogen atom (16 mg)
Quellen und Nachweise
- ORD-Eintrag
- ord-77dbcab9c8b4481aaacbf804ba142cb9
- Quelldatensatz
- uspto-grants-2010_04
- Patentnummer
- US07691893B2
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