4-(1,1-Dioxido-2-isothiazolidinyl)-1-(phenylmethyl)piperidine → 2-(piperidin-4-yl)-1lambda6,2-thiazolidine-1,1-dione
Reaktionsgleichung
[O:1]=[S:2]1(=[O:20])[CH2:6][CH2:5][CH2:4][N:3]1[CH:7]1[CH2:12][CH2:11][N:10](CC2C=CC=CC=2)[CH2:9][CH2:8]1>[OH-].[Pd+2].[OH-].CO>[O:20]=[S:2]1(=[O:1])[CH2:6][CH2:5][CH2:4][N:3]1[CH:7]1[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
20% Palladium hydroxide (100 mg) was added to the methanol solution (5 mL) containing 4-(1,1-dioxo-1λ6-isothiazolidin-2-yl)-1-benzylpiperidine (252 mg) at 0° C., followed by stirring at room temperature for 5 hrs. under a hydrogen atmosphere. The reaction mixture was filtered to remove the palladium catalyst, followed by concentration under reduced pressure to give the title compound.
Aufarbeitung
- filtrationThe reaction mixture was filtered
- customto remove the palladium catalyst
- concentrationfollowed by concentration under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-8989cc46dee44dd7a73021652d3582be
- Quelldatensatz
- uspto-grants-2010_04
- Patentnummer
- US07691860B2
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