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Pyridine → Benzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylate

HRID 1462035
ノート
印刷プレビュー

反応式

HRID 1462035 の反応式
P(Cl)(Cl)(Cl)(Cl)[Cl:2].N1C=CC=CC=1.O[CH2:14][C:15]1[CH2:16][S:17][C@@H:18]2[CH:38]([NH:39]C(=O)CC3C=CC=CC=3)[C:37](=[O:49])[N:19]2[C:20]=1[C:21]([O:23][CH:24]([C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:22].C(O)CCO>C(Cl)Cl>[NH2:39][CH:38]1[C:37](=[O:49])[N:19]2[C:20]([C:21]([O:23][CH:24]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)[C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[O:22])=[C:15]([CH2:14][Cl:2])[CH2:16][S:17][C@H:18]12
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 1049PyridineHCID 104421,3-PropanediolHCID 24819Phosphorus pentachlorideHCID 13339796Benzhydryl 3-hydroxymethyl-7-phenylacetamido-3-cephem-4-carboxylate

生成物 1

HCID 13239626Benzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylate収率 51%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

反応条件

温度
20 °C

実験手順

To a slurry of PCl5 (8.3 g, 40 mmoles) in CH2Cl2 (100 mL) was added pyridine (3.2 g, 40 mmoles) and the mixture was stirred for 20 minutes at 20° C. To the mixture was added benzhydryl 3-hydroxymethyl-7-phenylacetamido-3-cephem-4-carboxylate prepared in Preparation No. 3 (5.1 g, 10 mmoles) with stirring at -40° C., in one portion. The mixture was stirred at -10° C. for 15 minutes and allowed to stand at -10° C. to -15° C. for 7 hours. To the cooled solution (-20° C.) was added propane-1,3-diol (10 mL) and the mixture was allowed to stand at -20° C. for 16 hours and then at room temperature for 20 minutes with stirring. The resulting solution was washed with ice-water (2×20 mL) and saturated aqueous NaCl (10 mL), dried over MgSO4 and concentrated in vacuo. The gummy residue (12 g) was dissolved in a mixture of CHCl3 and n-hexane (2:1), and subjected to chromatography using a silica gel column (200 g) and the same solvent as eluant. Fractions containing the title compound were evaporated in vacuo and the residue triturated with n-hexane to give the title product (2.1 g, 51%), melting at >110° C. (dec.).

後処理

  1. customprepared in Preparation No
  2. stirringThe mixture was stirred at -10° C. for 15 minutes
  3. waitto stand at -10° C. to -15° C. for 7 hours
  4. waitto stand at -20° C. for 16 hours
  5. stirringat room temperature for 20 minutes with stirring
  6. washThe resulting solution was washed with ice-water (2×20 mL) and saturated aqueous NaCl (10 mL)
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated in vacuo
  9. dissolutionThe gummy residue (12 g) was dissolved in a mixture of CHCl3 and n-hexane (2:1)
  10. additionFractions containing the title compound
  11. customwere evaporated in vacuo
  12. customthe residue triturated with n-hexane

出典と根拠

ORDレコード
ord-15d6f7cef3884f868e7fa9fcaa082b3e
出典データセット
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04457929

反応ノート

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