HCID 69655555, compound → HCID 69655272, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:34])[CH:5]=[CH:6][C:7]1[C:12]([O:13][CH2:14][C:15]([N:17]2[CH2:22][C@H:21]([CH3:23])[N:20]([CH2:24][C:25]3[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=3)[CH2:19][C@H:18]2[CH3:32])=[O:16])=[CH:11][CH:10]=[C:9]([CH3:33])[N:8]=1)[CH3:2]>CCO.[Pt]=O>[CH2:1]([O:3][C:4](=[O:34])[CH2:5][CH2:6][C:7]1[C:12]([O:13][CH2:14][C:15]([N:17]2[CH2:22][C@H:21]([CH3:23])[N:20]([CH2:24][C:25]3[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=3)[CH2:19][C@H:18]2[CH3:32])=[O:16])=[CH:11][CH:10]=[C:9]([CH3:33])[N:8]=1)[CH3:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 3-(3-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-6-methyl-pyridin-2-yl)-acrylic acid ethyl ester (0.54 g, 1.15 mmol) in EtOH (5.0 mL) was added platinum oxide (0.050 g) and the mixture was hydrogenated at 45 psi for 90 minutes. The mixture was filtered through celite and concentrated in vacuo to give the title compound (0.50 g).
Workup
- filtrationThe mixture was filtered through celite and
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-6b530ae27a03433a835046ef5fcb8a26
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07098212B2
Reaction notes
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