Methanesulfonic Acid → HCID 86752152, Verbindung
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([CH3:12])(=[O:11])=[O:10])=[CH:5][C:4]=1[CH2:13][NH:14][C@H:15]1[CH:20]2[CH2:21][CH2:22][N:17]([CH2:18][CH2:19]2)[C@H:16]1[CH:23]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.[CH3:36][S:37]([OH:40])(=[O:39])=[O:38]>CC(C)=O>[S:37]([OH:40])(=[O:39])(=[O:38])[CH3:36].[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([CH3:12])(=[O:11])=[O:10])=[CH:5][C:4]=1[CH2:13][NH:14][C@H:15]1[CH:20]2[CH2:19][CH2:18][N:17]([CH2:22][CH2:21]2)[C@H:16]1[CH:23]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of (2S,3S)-N-(2-methoxy-5-methylsulfonylphenyl)methyl-2-diphenylmethyl-1-azabicyclo[2.2.2]octan-3-amine (400 mg, 0.82 mmol) in acetone (10 mL) was added methanesulfonic acid (0.41 mmol, 39.2 mg). The precipitated white solid was filtered off to give the title compound (218 mg, 30.3%, 1st crop).
Aufarbeitung
- filtrationThe precipitated white solid was filtered off
Quellen und Nachweise
- ORD-Eintrag
- ord-dc1de828b900414b9045f77505d1865d
- Quelldatensatz
- uspto-grants-1998_02
- Patentnummer
- US05721255
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