Water → HCID 58573496, compound
Reaction equation
[CH2:1]([C@@:4]1(C)[CH2:9][C@H:8]([C:10]2[CH:15]=[C:14]([F:16])[CH:13]=[C:12]([Cl:17])[CH:11]=2)[C@@H:7]([C:18]2[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][CH:19]=2)[N:6]([C@@H:25]([CH2:31][CH3:32])[CH2:26][S:27]([CH3:30])(=[O:29])=[O:28])[C:5]1=[O:33])C=C.O.I([O-])(=O)(=O)=O.[Na+].CC[O:44][C:45]([CH3:47])=[O:46]>C(#N)C.O.[Ru](Cl)(Cl)Cl>[Cl:17][C:12]1[CH:11]=[C:10]([C@@H:8]2[C@@H:7]([C:18]3[CH:19]=[CH:20][C:21]([Cl:24])=[CH:22][CH:23]=3)[N:6]([C@@H:25]([CH2:31][CH3:32])[CH2:26][S:27]([CH3:30])(=[O:28])=[O:29])[C:5](=[O:33])[C@:4]([CH2:47][C:45]([OH:44])=[O:46])([CH3:1])[CH2:9]2)[CH:15]=[C:14]([F:16])[CH:13]=1Participants
7
Procedure
To a solution of (3S,5R,6S)-3-allyl-5-(3-chloro-5-fluorophenyl)-6-(4-chlorophenyl)-3-methyl-1-((S)-1-(methylsulfonyl)butan-2-yl)piperidin-2-one (Example 395, Step B, 58 mg, 0.110 mmol) in acetonitrile (1.0 mL), EtOAc (1.0 mL), and water (1.5 mL) was added ruthenium(III) chloride hydrate (0.55 mg, 2.42 μmol) and sodium periodate (144 mg, 0.672 mmol). After 2 hours, the mixture was partitioned between water and EtOAc. The organic layer was washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by preparative thin layer chromatography on silica gel (eluent: 10% MeOH/DCM) to provide the title compound.
Workup
- customthe mixture was partitioned between water and EtOAc
- washThe organic layer was washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationthe filtrate was concentrated
- customThe residue was purified by preparative thin layer chromatography on silica gel (eluent: 10% MeOH/DCM)
Sources & evidence
- ORD record
- ord-1b7e49941a9d4f3abe6d7486163bdcf2
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09296736B2
Reaction notes
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