p-Toluenesulfonic acid monohydrate → HCID 86754641, Verbindung
Reaktionsgleichung
O.[C:2]1([CH3:12])[CH:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([N:20]2[CH2:24][CH2:23][C@H:22]([CH2:25][N:26]3[CH2:31][CH2:30][N:29]([CH2:32][CH2:33][O:34][CH3:35])[CH2:28][CH2:27]3)[C:21]2=[O:36])=[CH:16][CH:15]=1>C(OCC)(=O)C>[OH2:9].[OH2:34].[C:2]1([CH3:12])[CH:3]=[CH:4][C:5]([S:8]([OH:11])(=[O:9])=[O:10])=[CH:6][CH:7]=1.[C:2]1([CH3:12])[CH:3]=[CH:4][C:5]([S:8]([OH:11])(=[O:9])=[O:10])=[CH:6][CH:7]=1.[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([N:20]2[CH2:24][CH2:23][C@H:22]([CH2:25][N:26]3[CH2:27][CH2:28][N:29]([CH2:32][CH2:33][O:34][CH3:35])[CH2:30][CH2:31]3)[C:21]2=[O:36])=[CH:16][CH:15]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 380 mg of p-toluenesulfonic acid monohydrate in 10 mL of ethyl acetate was added a solution of 352 mg of (R)-1-(4-chlorophenyl)-3-(4-(2-methoxyethyl)piperazin-1-yl)methyl-2-pyrrolidinone in 10 mL of ethyl acetate. The mixture was stirred at room temperature and cooled. The precipitated solid was filtered and dried to give 712 mg of the title compound.
Aufarbeitung
- temperaturecooled
- filtrationThe precipitated solid was filtered
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-fda6ce23a59e4ff78afac8cf92d8a5bc
- Quelldatensatz
- uspto-grants-1999_10
- Patentnummer
- US05969138
Notizen zur Reaktion
Wird geladen…