Sodium periodate → HCID 178432825, compound
Reaction equation
[OH:1][C:2]1[CH:8]2[CH:6]([CH2:7]2)[C:5]([CH3:11])([S:9][CH3:10])[C:4](=[O:12])[C:3]=1[C:13]([C:15]1[C:16]([CH3:25])=[N:17][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:19][CH:20]=1)=[O:14].I([O-])(=O)(=O)=[O:27].[Na+]>CO>[OH:1][C:2]1[CH:8]2[CH:6]([CH2:7]2)[C:5]([S:9]([CH3:10])=[O:27])([CH3:11])[C:4](=[O:12])[C:3]=1[C:13]([C:15]1[C:16]([CH3:25])=[N:17][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:19][CH:20]=1)=[O:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.87 g (2.3 mmol) of 5-hydroxy-2-methyl-2-methylsulfanyl-4-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[4.1.0]hept-4-en-3-one (Compound A2-D113), dissolved in 8 ml of methanol, is warmed for 3 hours at a temperature of 50° C. in the presence of 0.56 g of sodium periodate. The mixture is then partitioned between ethyl acetate an d sodium chloride solution, concentrated, and the crude product is purified by chromatography (mobile phase: ethyl acetate/m ethanol 19:1). Pure 5-hydroxy-2-methanesulfinyl-2-methyl-4-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[4.1.0]hept-4-en-3-one is obtained as tautomer and isomer mixture of melting point 159.5-160° C.
Workup
- customThe mixture is then partitioned between ethyl acetate an d sodium chloride solution
- concentrationconcentrated
- customthe crude product is purified by chromatography (mobile phase: ethyl acetate/m ethanol 19:1)
Sources & evidence
- ORD record
- ord-378bdd8b893943338db42c6fb3df506b
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06534445B1
Reaction notes
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