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

HRID 1088099ノート

反応式

HRID 1088099 の反応式
O.NN.Cl.[NH2:5][O:6][CH2:7][C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:9].[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>[CH2:11]([O:10][C:8]([CH2:7][O:6][N:5]=[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:9])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

参加物

9

反応物 5

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 24654Hydrazine hydrate (1:1)HCID 11309879Benzyl 2-(aminooxy)acetateHCID 13116693(2-Formamido-1,3-thiazol-4-yl)(oxo)acetic acid

生成物 1

HCID 542157752-Benzyloxycarbonylmethoxyimino-2-(2-formamidothiazol-4-yl)acetic acid

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 1049Pyridine溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

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 benzyl 2-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.).

後処理

  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

出典と根拠

ORDレコード
ord-7880bc398b314201adec37077342932f
出典データセット
uspto-grants-1990_10
特許番号
US04960889

反応ノート

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