Water → HCID 178502650, compound

HRID 244950Notes

Reaction equation

HRID 244950 reaction equation
[OH:1][C:2]1[N:6]([C:7]([CH3:16])([CH3:15])[CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:5]=[C:4]([CH:17]([CH3:19])[CH3:18])[C:3]=1[C:20](=O)[CH3:21].Cl.[CH3:24][O:25][NH2:26].C([O-])(=O)C.[Na+].O>C(O)C>[CH3:24][O:25][N:26]=[C:20]([C:3]1[C:4]([CH:17]([CH3:19])[CH3:18])=[N:5][N:6]([C:7]([CH3:16])([CH3:15])[CH2:8][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:2]=1[OH:1])[CH3:21]

Participants

6

Procedure

150 mg (0.50 mmol) of 1-(5-hydroxy-3-isopropyl-1-(2-methyl-1-phenylpropan-2-yl)-1H-pyrazol-4-yl)ethanone, 209 mg (2.50 mmol) of methoxyamine hydrochloride and 286 mg (3.49 mmol) of sodium acetate were mixed with 1.3 ml of distilled water and 1.3 ml of ethanol and stirred at room temperature for 16 hours. After completion of the reaction, the reaction solution was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (silica gel 4 g, ethyl acetate:hexane=1:99) to give 70 mg of the desired product as an orange oil.

Workup

  1. customAfter completion of the reaction
  2. extractionthe reaction solution was extracted with ethyl acetate
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe resulting residue was purified by silica gel column chromatography (silica gel 4 g, ethyl acetate:hexane=1:99)

Sources & evidence

ORD record
ord-0f2dfd61e23b4057ba72486a910ddffa
Source dataset
uspto-grants-2014_02
Patent number
US08658686B2

Reaction notes

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