Sodium Hydroxide → HCID 54045511, compound

HRID 1075259Notes

Reaction equation

HRID 1075259 reaction equation
C(NC1C=CN=C(C(=O)C(SC)=O)C=1)=O.[OH-].[Na+].[CH:18]([NH:20][C:21]1[CH:26]=[CH:25][N:24]=[C:23]([C:27](=O)[C:28]([OH:30])=[O:29])[CH:22]=1)=[O:19].Cl.[CH3:33][O:34][NH2:35]>CO>[CH:18]([NH:20][C:21]1[CH:26]=[CH:25][N:24]=[C:23]([C:27](=[N:35][O:34][CH3:33])[C:28]([OH:30])=[O:29])[CH:22]=1)=[O:19]

Participants

6

Procedure

A mixture of S-methyl 2-(4-formamidopyridin-2-yl)thioglyoxylate (1.07 g.), methanol (20 ml.) and 1 N aqueous solution of sodium hydroxide (5.7 ml.) was stirred for 50 minutes at ambient temperature to give a solutions containing 2-(4-formamidopyridin-2-yl)glyoxylic acid. To the solution was added O-methylhydroxylamine hydrochloride (438 mg.), and the mixture was stirred for an hour at ambient temperature. After the removal of the solvent from the reaction mixture, to the residue was added water (5 ml.), and the mixture was washed with ethyl acetate and then water was distilled off. The remaining water in the residue was azeotropically removed with ethanol and benzene in turn to give a pale brown powder of 2-(4-formamidopyridin-2-yl)-2-methoxyiminoacetic acid (syn isomer) (960 mg.).

Workup

  1. customto give a solutions
  2. stirringthe mixture was stirred for an hour at ambient temperature
  3. customAfter the removal of the solvent from the reaction mixture
  4. additionto the residue was added water (5 ml.)
  5. washthe mixture was washed with ethyl acetate
  6. distillationwater was distilled off
  7. customThe remaining water in the residue was azeotropically removed with ethanol and benzene in turn

Sources & evidence

ORD record
ord-e870f19c96824da096f56386c601fcf7
Source dataset
uspto-grants-1983_07
Patent number
US04395411

Reaction notes

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