Water → 1-[4-(4-Fluoro-phenyl)-1-methyl-1H-pyrazol-3-yl]-1-((S)-2-{[5-(1-hydroxy-ethyl)-pyrimidin-2-ylamino]-methyl}-piperidin-1-yl)-methanone
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:14]([N:16]3[CH2:21][CH2:20][CH2:19][CH2:18][C@H:17]3[CH2:22][NH:23][C:24]3[N:29]=[CH:28][C:27]([C:30](=[O:32])[CH3:31])=[CH:26][N:25]=3)=[O:15])=[N:10][N:11]([CH3:13])[CH:12]=2)=[CH:4][CH:3]=1.[BH4-].[Na+].O>CO>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:9]([C:14]([N:16]3[CH2:21][CH2:20][CH2:19][CH2:18][C@H:17]3[CH2:22][NH:23][C:24]3[N:25]=[CH:26][C:27]([CH:30]([OH:32])[CH3:31])=[CH:28][N:29]=3)=[O:15])=[N:10][N:11]([CH3:13])[CH:12]=2)=[CH:6][CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1-{2-[((S)-1-{1-[4-(4-Fluoro-phenyl)-1-methyl-1H-pyrazol-3-yl]-methanoyl}-piperidin-2-ylmethyl)-amino]-pyrimidin-5-yl}-ethanone (0.2 g) was dissolved in methanol 20 ml) and sodium borohydride (0.4 g) added. The reaction was stirred overnight, water was added and stirring continued for 30 min. The reaction mixture was extracted with ethyl acetate (x3), the organic extracts combined, dried (MgSO4) and solvent removed at reduced pressure to give the title compound as a colourless foam.
Workup
- additionadded
- stirringstirring
- waitcontinued for 30 min
- extractionThe reaction mixture was extracted with ethyl acetate (x3)
- dry with materialdried (MgSO4) and solvent
- customremoved at reduced pressure
Sources & evidence
- ORD record
- ord-5050cd275b4c48fd9ee56a3f15b226fc
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07741329B2
Reaction notes
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