Sodium Hydroxide → HCID 54045511, compound

HRID 1982689Notes

Reaction equation

HRID 1982689 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 1N 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-f86f137d33434544a3563f0f830c8703
Source dataset
uspto-grants-1986_06
Patent number
US04596869

Reaction notes

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