Methyl morpholine oxide → HCID 58763943, compound

HRID 859185Notes

Reaction equation

HRID 859185 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:10]([O:11][CH2:12][CH:13]=C)=[C:9]([C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=2)[N:8]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[Cl:28])[N:7]=1)=[O:5])[CH3:2].C[N+]1([O-])CC[O:33]CC1.I([O-])(=O)(=O)=O.[Na+]>O.O1CCOCC1.C(OCC)(=O)C>[CH2:1]([O:3][C:4]([C:6]1[C:10]([O:11][CH2:12][CH:13]=[O:33])=[C:9]([C:15]2[CH:16]=[CH:17][C:18]([Cl:21])=[CH:19][CH:20]=2)[N:8]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[Cl:28])[N:7]=1)=[O:5])[CH3:2]

Participants

7

Procedure

To a stirred solution of 4-allyloxy-5-(4-chlorophenyl)-1-(2-chlorophenyl)-1H-pyrazole-3-carboxylic acid ethyl ester I-1e (337 mg, 0.8 mmol) osmium tetroxide (53 microliters of a 0.15 M solution in water) and N-methylmorpholine-N-oxide (120 mg, 0.9 mmol) in dioxane (2.4 ml)/water (0.6 ml) was stirred at ambient temperature for 18 hours, then sodium periodate (1.7 g, 8.1 mmol) was added and stirring was continued for 3.5 hours. The thick slurry was diluted with ethyl acetate (100 ml), filtered and solids washed 2× with ethyl acetate. The combined filtrates were washed with water, brine, dried (Na2SO4) and concentrated in vacuo to afford an oil. Silica gel chromatography (25% ethyl acetate/hexanes) afforded the title compound (I-1f) as a colorless foam, 130 mg.

Workup

  1. filtrationfiltered
  2. washsolids washed 2× with ethyl acetate
  3. washThe combined filtrates were washed with water, brine
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated in vacuo
  6. customto afford an oil

Sources & evidence

ORD record
ord-8044a58e722e4fbf970487ee56b6d4a3
Source dataset
uspto-grants-2006_12
Patent number
US07151097B2

Reaction notes

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