Water → HCID 57075227, compound

HRID 1603962Notes

Reaction equation

HRID 1603962 reaction equation
[CH2:1]([O:8][N:9]=[CH:10][O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[C:19](=[N:24][O:25][CH3:26])[C:20]([O:22]C)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:27][NH2:28].O>CO>[CH3:27][NH:28][C:20](=[O:22])[C:19]([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[CH2:12][O:11][CH:10]=[N:9][O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[N:24][O:25][CH3:26]

Participants

5

Procedure

Methyl 2-(2-benzyloxyiminomethyloxymethylphenyl)-2-methoxyiminoacetate) (compound No. 2) (200 mg. 0.6 mmol) was dissolved into 8 ml of methanol, an aqueous solution of 40% methylamine (230 mg, 2.9 mmol) was added thereto. After stirring for 1 day, water was added to the reaction solution, methanol was removed by evaporation, and there was extracted with ethyl acetate. The organic layer was rinsed with water and dried. After removing the solvent by evaporation, the residue was purified with silica gel chromatography to obtain 0.18 g of N-methyl 2-(2-benzyloxyiminomethyloxymethylphenyl)-2-methoxyiminoacetamide (Compound No. 3; yield: 90%). The proton NMR spectrum of the compound is 2.81 s (3H); 3.89 s (3H); 4.91 s (2H); 5.00 s (2H); 6.52 s (1H): 6.82 bd(1H); 7.15-7.21 m (1H); 7.23-7.47 m (8H) (solvent: CDCl3).

Workup

  1. customwas removed by evaporation, and there
  2. extractionwas extracted with ethyl acetate
  3. washThe organic layer was rinsed with water
  4. customdried
  5. customAfter removing the solvent
  6. customby evaporation
  7. customthe residue was purified with silica gel chromatography

Sources & evidence

ORD record
ord-4e155b93ebd84f9fbd9d2809e373c4a1
Source dataset
uspto-grants-1999_11
Patent number
US05990161

Reaction notes

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