Aluminum(III) Chloride → HCID 178516324, 화합물

HRID 249617노트

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HRID 249617 반응식
C1(C([O:14][C:15]([C:17]2[N:22]3[C:23](=[O:63])[C@@H:24](NC(=O)/C(/C4N=C(NC(OC(C)(C)C)=O)SC=4)=N\OC(C4C=CC=CC=4)(C4C=CC=CC=4)C4C=CC=CC=4)[C@H:21]3[S:20][CH2:19][C:18]=2[CH2:64][S:65][C:66]2[N:67]=[N:68][NH:69][CH:70]=2)=[S:16])C2C=CC=CC=2)C=CC=CC=1.[Cl-].[Al+3].[Cl-].[Cl-]>C1(OC)C=CC=CC=1.[N+](C)([O-])=O>[NH:69]1[CH:70]=[C:66]([S:65][CH2:64][C:18]2[CH2:19][S:20][C@@H:21]3[CH2:24][C:23](=[O:63])[N:22]3[C:17]=2[C:15]([OH:14])=[S:16])[N:67]=[N:68]1

참가 물질

5

실험 절차

To a suspension of 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol -4- yl)-2-trityloxyiminoacetamido]-3-(1,2,3-triazol-4-yl) thiomethylthio-3- cephem-4-carboxylic acid diphenylmethyl ester (9.2 g: 9 mMol.) in a mixture of anisole (18 ml) and nitromethane (72 ml) is added dropwise a solution of aluminum chloride (9.6 g: 72 mMol.) in anisole (31 ml) at -30° C. After stirring for 1 hour at the same temperature, the reaction mixture is quenched with ethanol (25 ml), stirred for several minutes, diluted with 1N-hydrochloric acid (75 ml) and water (500 ml), and washed with ethyl acetate. The aqueous layer was separated, concentrated to remove the organic solvents, and passed through a column of styrene- divinylbenzene copolymer adsorbent. The product is eluted with a mixture of methanol and water (4:1) to give 7β-(Z)-2-(2-aminothiazol-4-yl)-2-hydroxyiminoacetamido]-3-(1,2,3-triazol-4-yl)thiomethylthio -3-cephem-4-carboxylic acid as pale yellow powder (4.19 g). Yield: 90%.

후처리

  1. customthe reaction mixture is quenched with ethanol (25 ml)
  2. stirringstirred for several minutes
  3. additiondiluted with 1N-hydrochloric acid (75 ml) and water (500 ml)
  4. washwashed with ethyl acetate
  5. customThe aqueous layer was separated
  6. concentrationconcentrated
  7. customto remove the organic solvents
  8. washThe product is eluted with a mixture of methanol and water (4:1)

출처 및 근거

ORD 기록
ord-c6b8e3efd4634cb9ab33f3af0092d8fd
출처 데이터셋
uspto-grants-1993_05
특허 번호
US05214037

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