Hydrochloric Acid → HCID 14854210、化合物

HRID 329794

反応式

HRID 329794 の反応式
[C:1]([O:5][C:6]([NH:8][C@@H:9]1[C:29](=[O:30])[N:11]2[C:12]([C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])=[C:13]([C:16]([O:18]CC=C)=[O:17])[CH2:14][CH2:15][C@H:10]12)=[O:7])([CH3:4])([CH3:3])[CH3:2].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[SnH](CCCC)(CCCC)CCCC.Cl>CC#N.CCOCC.O.C(Cl)(Cl)Cl>[C:1]([O:5][C:6]([NH:8][C@@H:9]1[C:29](=[O:30])[N:11]2[C:12]([C:22]([O:24][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:23])=[C:13]([C:16]([OH:18])=[O:17])[CH2:14][CH2:15][C@H:10]12)=[O:7])([CH3:4])([CH3:2])[CH3:3]

参加物

8

反応条件

温度
0 °C

実験手順

To 700 mg (1.657 mMol) of 4-t-butyl 7β-t-butyloxycarbonylamino-3-allyloxycarbonyl-1-carba-3-cephem-4-carboxylate, dissolved in 12 ml of (1:1) CH3CN/(CH3CH2)2O, was added 174 mg (0.663 mMol) of triphenylphosphine and 20.34 mg (0.0829 mMol) of ##STR153## The reaction mixture was stirred for approximately 20 minutes and then cooled to 0° C. and treated with 0.464 ml (1.724 l) of (CH3CH2CH2CH2)3SnH. The reaction mixture was then allowed to cool and stirring was continued for 50 minutes. The crude reaction mixture was then treated with 1N HCl. This mixture was then poured into 100 ml of CHCl3 and 25 ml of H2O. The organic layer was separated, dried over anhydrous MgSO4, filtered, and concentrated, under reduced pressure to provide an oily solid. The crude product was recrystallized from CH2Cl2 /hexane to yield 570 mg (90%) of the title compound.

後処理

  1. temperatureto cool
  2. stirringstirring
  3. waitwas continued for 50 minutes
  4. customThe crude reaction mixture
  5. customThe organic layer was separated
  6. dry with materialdried over anhydrous MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated, under reduced pressure
  9. customto provide an oily solid
  10. customThe crude product was recrystallized from CH2Cl2 /hexane

出典と根拠

ORDレコード
ord-8c4ecdf71a2946e985d12e9cb2ad5e2c
出典データセット
uspto-grants-1990_01
特許番号
US04892942

関連ノート

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