Hydrochloric Acid → 2-Benzyloxycarbonylmethoxyimino-2-(2-formamidothiazol-4-yl)acetic acid

HRID 905417Notes

Reaction equation

HRID 905417 reaction equation
O.NN.Cl.[CH2:5]([O:12][C:13](=[O:17])[CH2:14][O:15][NH2:16])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[CH:18]([NH:20][C:21]1[S:22][CH:23]=[C:24]([C:26](=O)[C:27]([OH:29])=[O:28])[N:25]=1)=[O:19].[OH-].[Na+]>CO.O1CCCC1.N1C=CC=CC=1>[CH2:5]([O:12][C:13]([CH2:14][O:15][N:16]=[C:26]([C:24]1[N:25]=[C:21]([NH:20][CH:18]=[O:19])[S:22][CH:23]=1)[C:27]([OH:29])=[O:28])=[O:17])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

Participants

9

Procedure

A solution of hydrazine hydrate (8.0 g) in methanol (16 ml) was added to a suspension of benzyl 2-phthalimidoxyacetate (46.0 g) in tetrahydrofuran (150 ml), and the mixture was stirred at ambient temperature for 30 minutes. To the reaction mixture was added 20% hydrochloric acid under ice-cooling, followed by stirring at the same temperature for 10 minutes. The insoluble substance was filtered off to give a solution containing benzyl2-aminooxyacetate. To this solution were added (2-formamidothiazol-4-yl)glyoxylic acid (24.7 g) and pyridine (24.8 ml), and the mixture was stirred at ambient temperature for 3 hours. The reaction mixture was adjusted to pH 7.5 with 10% aqueous sodium hydroxide and then washed with ethyl acetate. The resultant aqueous solution was acidified to pH 2.0 with 10% hydrochloric acid, followed by extraction with ethyl acetate. The extract was washed with an aqueous sodium chloride and then dried over magnesium sulfate. The solution was evaporated and the residue was pulverized with diisopropyl ether to give 2-benzyloxycarbonylmethoxyimino-2-(2-formamidothiazol-4-yl)acetic acid (syn isomer) (37 g), mp 152° C. (dec.).

Workup

  1. temperaturecooling
  2. stirringby stirring at the same temperature for 10 minutes
  3. filtrationThe insoluble substance was filtered off
  4. customto give a solution
  5. stirringthe mixture was stirred at ambient temperature for 3 hours
  6. washwashed with ethyl acetate
  7. extractionfollowed by extraction with ethyl acetate
  8. washThe extract was washed with an aqueous sodium chloride
  9. dry with materialdried over magnesium sulfate
  10. customThe solution was evaporated

Sources & evidence

ORD record
ord-8cbe6b1dfc01471d94e390d5846d9f9e
Source dataset
uspto-grants-1983_12
Patent number
US04423213

Reaction notes

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