m-Chloroperbenzoic acid → Methyl 2-fluoro-4-[3-(methylsulfinyl)-1,2,4-triazin-6-yl]benzoate
Reaction equation
[F:1][C:2]1[CH:11]=[C:10]([C:12]2[N:17]=[N:16][C:15]([S:18][CH3:19])=[N:14][CH:13]=2)[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].ClC1C=CC=C(C(OO)=[O:28])C=1>C(Cl)Cl>[F:1][C:2]1[CH:11]=[C:10]([C:12]2[N:17]=[N:16][C:15]([S:18]([CH3:19])=[O:28])=[N:14][CH:13]=2)[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]Participants
4
Procedure
To a cooled (0° C.) solution of methyl 2-fluoro-4-[3-(methylthio)-1,2,4-triazin-6-yl]benzoate (0.180 g, 0.000644 mol) in methylene chloride (10 mL) was added m-chloroperbenzoic acid (0.32 g, 0.0014 mol) in DCM (3 ml) with stirring. The mixture was stirred at 0° C. for 1.5 h, and diluted with DCM. The resulting solution was quenched with saturated Na2S2O3 solution. After separation the organic layer was washed with saturated NaHCO3 solution, brine; and dried over Na2SO4. After filtration the filtrate was concentrated to yield nearly quantitative product which was directly used in the next step without further purification. Analytical LCMS: (M+H)+=296.0.
Workup
- stirringThe mixture was stirred at 0° C. for 1.5 h
- customThe resulting solution was quenched with saturated Na2S2O3 solution
- customAfter separation the organic layer
- washwas washed with saturated NaHCO3 solution, brine
- dry with materialand dried over Na2SO4
- filtrationAfter filtration the filtrate
- concentrationwas concentrated
- customto yield nearly quantitative product which
- customwas directly used in the next step without further purification
Sources & evidence
- ORD record
- ord-e6e49767518749d69d861dddd51c10d5
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07683060B2
Reaction notes
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