Hydrochloric Acid → 1-{[4-Ethoxycarbonylamino-1-(2-methyl-4-pyridyl)-4-piperidinyl]methyl}-2-piperazinone Hydrochloride
Reaktionsgleichung
[ClH:1].C(OC([N:12]1[CH2:17][CH2:16][N:15]([CH2:18][C:19]2([NH:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH2:24][CH2:23][N:22]([C:25]3[CH:30]=[CH:29][N:28]=[C:27]([CH3:31])[CH:26]=3)[CH2:21][CH2:20]2)[C:14](=[O:38])[CH2:13]1)=O)C1C=CC=CC=1>C(OCC)(=O)C.C(O)C.[C].[Pd]>[ClH:1].[CH2:36]([O:35][C:33]([NH:32][C:19]1([CH2:18][N:15]2[CH2:16][CH2:17][NH:12][CH2:13][C:14]2=[O:38])[CH2:20][CH2:21][N:22]([C:25]2[CH:30]=[CH:29][N:28]=[C:27]([CH3:31])[CH:26]=2)[CH2:23][CH2:24]1)=[O:34])[CH3:37]Komponenten
6
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
A 4N hydrochloric acid solution in ethyl acetate (0.7 ml) and 10% palladium carbon (500 mg) were added to a solution of 4-benzyloxycarbonyl-1-{[4-ethoxycarbonylamino-1-(2-methyl-4-pyridyl)-4-piperidiny]methyl}-2-piperazinone (1.3 g) in ethanol (50 ml), and the mixture was stirred at room temperature for 15 hours under a nitrogen atmosphere. After the catalyst was removed, the solvent was distilled off to obtain the colorless amorphous title compound (1.15 g).
Aufarbeitung
- customAfter the catalyst was removed
- distillationthe solvent was distilled off
Quellen und Nachweise
- ORD-Eintrag
- ord-8343bc83656e49de9df0f978d4087a83
- Quelldatensatz
- uspto-grants-2006_09
- Patentnummer
- US07109200B2
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