Trifluoroacetic acid → 7-Amino-3vinyl-3-cephem-4-carboxylic acid

HRID 647684

반응식

HRID 647684 반응식
C(=[N:8][CH:9]1[C:34](=[O:35])[N:11]2[C:12]([C:18]([O:20]C(C3C=CC=CC=3)C3C=CC=CC=3)=[O:19])=[C:13]([CH:16]=[CH2:17])[CH2:14][S:15][C@H:10]12)C1C=CC=CC=1.FC(F)(F)C(O)=O.C(=O)(O)[O-].[Na+].C(=O)([O-])[O-].[Na+].[Na+]>C1(OC)C=CC=CC=1.C(OCC)(=O)C>[NH2:8][CH:9]1[C:34](=[O:35])[N:11]2[C:12]([C:18]([OH:20])=[O:19])=[C:13]([CH:16]=[CH2:17])[CH2:14][S:15][C@H:10]12

참가 물질

7

실험 절차

To a suspension of benzhydryl 7-benzylideneamino-3-vinyl-3-cephem-4-carboxylate (8.6 g) in anisole (10 ml) was added dropwise trifluoroacetic acid (10 ml) at -20° C., and the reaction temperature was gradually raised to ambient temperature with stirring, followed by stirring at ambient temperature for half an hour. The reaction mixture was poured into a mixture of ethyl acetate (100 ml) and a saturated aqueous sodium bicarbonate (100 ml), and then the mixture was adjusted to pH 7.5 with 20% aqueous sodium carbonate. The separated aqueous solution was washed with ethyl acetate (100 ml) and adjusted to pH 7.2 with conc. hydrochloric acid, followed by subjecting to column chromatography on alumina (10 ml). Elution was carried out with 15% aqueous sodium chloride, and fractions containing a desired compound were collected and then adjusted to pH 3.3 with conc. hydrochloric acid. The precipitated crystals were collected by filtration, washed with acetone and dried to obtain 7-amino-3-vinyl-3-cephem-4-carboxylic acid (2.0 g), mp 200°-230° C. (dec.).

후처리

  1. stirringby stirring at ambient temperature for half an hour
  2. washThe separated aqueous solution was washed with ethyl acetate (100 ml)
  3. washElution
  4. additioncontaining a desired compound
  5. customwere collected
  6. filtrationThe precipitated crystals were collected by filtration
  7. washwashed with acetone
  8. customdried

출처 및 근거

ORD 기록
ord-06c9b378f5a24f0d8d2c66c4312a8f9f
출처 데이터셋
uspto-grants-1983_10
특허 번호
US04409214

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