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Diketene → 7-Acetoacetamido-3-acetoxymethyl-3-cephem-4-carboxylic acid

HRID 1979796
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HRID 1979796 반응식
[CH3:1][C:2]([O:4][CH2:5][C:6]1[CH2:15][S:14][C@@H:9]2[C@H:10]([NH2:13])[C:11](=[O:12])[N:8]2[C:7]=1[C:16]([OH:18])=[O:17])=[O:3].[CH2:19]=[C:20]1[O:24][C:22](=[O:23])[CH2:21]1>[OH-].[Na+].C(OCC)(=O)C>[C:2]([O:4][CH2:5][C:6]1[CH2:15][S:14][C@@H:9]2[CH:10]([NH:13][C:22](=[O:23])[CH2:21][C:20](=[O:24])[CH3:19])[C:11](=[O:12])[N:8]2[C:7]=1[C:16]([OH:18])=[O:17])(=[O:3])[CH3:1]
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참가 물질

5

반응물 2

HCID 12661DiketeneHCID 4413287-Aminocephalosporanic acid

생성물 1

HCID 887151507-Acetoacetamido-3-acetoxymethyl-3-cephem-4-carboxylic acid수율 61.8%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 14798Sodium Hydroxide용매

실험 절차

5.44 g of 7-aminocephalosporanic acid were dissolved in 20 ml of a 1N aqueous solution of sodium hydroxide, and 1.68 g of diketene were added, with ice-cooling, to the resulting solution. The mixture was stirred at the same temperature for 1 hour, after which it was diluted with 20 ml of ethyl acetate and then acidified. The mixture was extracted twice with ethyl acetate and the combined extracts were washed with an aqueous solution of sodium chloride, dehydrated over anhydrous magnesium sulphate and then concentrated by evaporation under reduced pressure, giving 4.4 g of the title compound as crystals melting at 150° C. (with decomposition).

후처리

  1. additionwere added, with ice-
  2. temperaturecooling, to the resulting solution
  3. extractionThe mixture was extracted twice with ethyl acetate
  4. washthe combined extracts were washed with an aqueous solution of sodium chloride
  5. concentrationconcentrated by evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-65c8e675f64c4b7191e5380d3f65b0ad
출처 데이터셋
uspto-grants-1984_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04482710

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