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Water → HCID 14180543、化合物

HRID 1905012
ノート
印刷プレビュー

反応式

HRID 1905012 の反応式
[O:1]([CH2:8][C:9]([NH:11][C@@H:12]1[C:50](=[O:51])[N:14]2[C:15]([C:34]([O:36][CH:37]([C:44]3[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=3)[C:38]3C=CC=[CH:40][CH:39]=3)=[O:35])=[C:16](OP(C3C=CC=CC=3)(C3C=CC=CC=3)=O)[CH2:17][S:18][C@H:13]12)=[O:10])C1C=CC=CC=1.[SH-:52].[Na+].O>CN(C)C=O.C(N(C(C)C)CC)(C)C>[O:1]([CH2:8][C:9]([NH:11][C@@H:12]1[C:50](=[O:51])[N:14]2[C:15]([C:34]([O:36][CH:37]([C:44]3[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=3)[C:38]3[CH:39]=[CH:40][CH:50]=[CH:12][CH:13]=3)=[O:35])=[C:16]([SH:52])[CH2:17][S:18][C@H:13]12)=[O:10])[C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 28015Sodium hydrosulfideHCID 14535654HCID 14535654、化合物

生成物 1

HCID 14180543HCID 14180543、化合物収率 170.7%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒2 回HCID 81531Diisopropylethylamine
溶媒

実験手順

To a solution of 16.4 g (21.9 mM) of benzhydryl 7β-phenoxyacetamido-3-diphenylphosphoryloxy-3-cephem-4-carboxylate in 128 ml of N,N-dimethylformamide were added at -10° C. a solution of 1.93 g (24.1 mM) of 70% sodium hydrosulfide in 86 ml of N,N-dimethylformamide and 4.25 g (32.9 mM) of diisopropylethylamine, and the mixture was stirred for 45 minutes. After the reaction, 200 ml of water was added and the mixture was extracted with 200 ml of diethyl ether. The aqueous layer was adjusted to pH 2 to 3 with 0.5% hydrochloric acid and extracted with ethyl acetate (300 ml), and the extract was washed with a saturated aqueous sodium chloride solution (200 ml×2) and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was chromatographed over silica gel column (eluent; ethyl acetate:benzene=1:2 to 2:1) to give 10.4 g of benzhydryl 7β -phenoxyacetamido-3-mercapto-3-cephem-4-carboxylate.

後処理

  1. additionwas added
  2. extractionthe mixture was extracted with 200 ml of diethyl ether
  3. extractionextracted with ethyl acetate (300 ml)
  4. washthe extract was washed with a saturated aqueous sodium chloride solution (200 ml×2)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customThe solvent was evaporated
  7. customthe residue was chromatographed over silica gel column (eluent; ethyl acetate:benzene=1:2 to 2:1)

出典と根拠

ORDレコード
ord-443febd636354cfc90f3ac65c9aa701f
出典データセット
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04841044

反応ノート

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