HCID 59327108, compound → HCID 59326867, compound
Reaction equation
[O:1]1[CH2:6][CH:5]=[C:4]([C:7]2[C:8]([O:13][C:14]3[CH:19]=[CH:18][C:17]([C:20]([C:22]4[NH:23][C:24]5[C:25]([N:30]=4)=[N:26][CH:27]=[CH:28][CH:29]=5)=[O:21])=[CH:16][CH:15]=3)=[N:9][CH:10]=[CH:11][CH:12]=2)[CH2:3][CH2:2]1>C1COCC1.[OH-].[Pd+2].[OH-]>[NH:23]1[C:24]2[C:25](=[N:26][CH:27]=[CH:28][CH:29]=2)[N:30]=[C:22]1[CH:20]([C:17]1[CH:18]=[CH:19][C:14]([O:13][C:8]2[C:7]([CH:4]3[CH2:5][CH2:6][O:1][CH2:2][CH2:3]3)=[CH:12][CH:11]=[CH:10][N:9]=2)=[CH:15][CH:16]=1)[OH:21]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a round bottomed flask was added (4-(3-(3,6-dihydro-2H-pyran-4-yl)pyridin-2-yloxy)phenyl)(1H-imidazo[4,5-b]pyridin-2-yl)methanone (0.3642 g, 0.914 mmol) in THF (3.05 mL). Palladium hydroxide (0.032 g, 0.046 mmol) was added. The round bottomed flask was flushed with N2(g) followed by vacuum repeating the process three times. A balloon of H2(g) was then added to the reaction. Upon completion, reaction was filtered. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Biotage pre-packed silica gel column (40S), eluting with a gradient of 0.5% to 10% MeOH in DCM, to provide (1H-imidazo[4,5-b]pyridin-2-yl)(4-(3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yloxy)phenyl)methanol. MS (ESI, pos. ion) m/z: 403.0 (M+1).
Workup
- customThe round bottomed flask was flushed with N2(g)
- additionA balloon of H2(g) was then added to the reaction
- customUpon completion, reaction
- filtrationwas filtered
- customchromatographed through a Biotage pre-packed silica gel column (40S)
- washeluting with a gradient of 0.5% to 10% MeOH in DCM
Sources & evidence
- ORD record
- ord-cadb5c4673b2416a8b4c4ab55c5abb49
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08759532B2
Reaction notes
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