(R)-benzyl 1-(2-(2-(tert-butoxycarbonylamino)acetoxy)propyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylate → (R)-1-(2-(2-(tert-butoxycarbonylamino)acetoxy)propyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylic acid
Reaktionsgleichung
[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]([O:12][C@H:13]([CH3:38])[CH2:14][N:15]1[C:19]([CH3:20])=[C:18]([C:21]([O:23]CC2C=CC=CC=2)=[O:22])[C:17](=[O:31])[N:16]1[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2]>CO.[Pd]>[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]([O:12][C@H:13]([CH3:38])[CH2:14][N:15]1[C:19]([CH3:20])=[C:18]([C:21]([OH:23])=[O:22])[C:17](=[O:31])[N:16]1[C:32]1[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=1)=[O:11])=[O:7])([CH3:2])([CH3:3])[CH3:4]Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of (R)-benzyl 1-(2-(2-(tert-butoxycarbonylamino)acetoxy)propyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylate (485 mg, 0.926 mmol) and 10% Pd/C (60 mg) in methanol (8 mL) was stirred for 3 h at rt. TLC analysis showed that the starting material was consumed completely. The catalyst was removed by filtration and the reaction mixture was concentrated in vacuo. The residue was purified by a silica gel column chromatography (100% EtOAc) to afford the title compound as a yellow solid (172 mg, 43% yield).
Aufarbeitung
- customwas consumed completely
- customThe catalyst was removed by filtration
- concentrationthe reaction mixture was concentrated in vacuo
- customThe residue was purified by a silica gel column chromatography (100% EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-662fe006018446ee82a36afc311c9ac7
- Quelldatensatz
- uspto-grants-2012_07
- Patentnummer
- US08232294B2
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