Hydrochloric Acid → 1-[5-(3'-Chloro-2-fluoro-6-methoxy-biphenyl-3-ylmethyl)-pyridin-2-yl]-ethylamine dihydrochloride
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[C:10]([CH2:16][C:17]3[CH:18]=[CH:19][C:20]([CH:23]([NH2:25])[CH3:24])=[N:21][CH:22]=3)[C:9]=2[F:26])[CH:5]=[CH:6][CH:7]=1.O1CCOCC1.[ClH:33]>C(OCC)C>[ClH:1].[ClH:33].[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[C:10]([CH2:16][C:17]3[CH:18]=[CH:19][C:20]([CH:23]([NH2:25])[CH3:24])=[N:21][CH:22]=3)[C:9]=2[F:26])[CH:5]=[CH:6][CH:7]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In an 8 mL vial equipped with a stir bar was placed 1-[5-(3′-Chloro-2-fluoro-6-methoxy-biphenyl-3-ylmethyl)-pyridin-2-yl]-ethylamine (P-606, 115 mg, 0.311 mmol), diethyl ether (3 mL), 1,4-dioxane (300 uL) and 2M HCl in diethyl ether (600 uL). The mixture was stirred at ambient temperature for 15 minutes, the solid was collected, washed with diethyl ether (3 mL) and dried to produce 98 mg of P-606-diHCl as a light tan solid in 71% yield.
Aufarbeitung
- customIn an 8 mL vial equipped with a stir bar
- customthe solid was collected
- washwashed with diethyl ether (3 mL)
- customdried
- customto produce 98 mg of P-606-diHCl as a light tan solid in 71% yield
Quellen und Nachweise
- ORD-Eintrag
- ord-f49fd974c5a04702a2985e5fe501aeed
- Quelldatensatz
- uspto-grants-2014_07
- Patentnummer
- US08791267B2
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