Tetrahydrofuran → 6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penam

HRID 1448373Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1448373
O1CCCC1.[C:6]1([C:12]([NH:25][CH:26]2[C:44](=[O:45])[N:28]3[CH:29]([C:34]4[N:38](C(OCC)=O)[N:37]=[N:36][N:35]=4)[C:30]([CH3:33])([CH3:32])[S:31][C@H:27]23)([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>O>[C:6]1([C:12]([NH:25][CH:26]2[C:44](=[O:45])[N:28]3[CH:29]([C:34]4[NH:35][N:36]=[N:37][N:38]=4)[C:30]([CH3:32])([CH3:33])[S:31][C@H:27]23)([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

Komponenten

4

Versuchsvorschrift

To a stirred mixture of 2 ml. of tetrahydrofuran and 4 ml. of water is added 150 mg. of 6-(triphenylmethylamino)-2,2-dimethyl-3-(1-[ethoxycarbonyl]tetrazol-5-yl)penam. The pH of the mixture is adjusted to 9.5, and stirring is continued at that pH for a further 30 minutes, at ambient temperature. The bulk of the tetrahydrofuran is removed by evaporation in vacuo, and the residue is portioned between water and ethyl acetate at pH 9. The ethyl acetate is removed and discarded. Fresh ethyl acetate is added and the pH is adjusted to 2.0. The ethyl acetate layer is removed, washed with water, dried using anhydrous sodium sulfate, and evaporated in vacuo to give the crude title compound.

Aufarbeitung

  1. additionTo a stirred mixture of 2 ml
  2. customThe bulk of the tetrahydrofuran is removed by evaporation in vacuo
  3. customThe ethyl acetate is removed
  4. additionFresh ethyl acetate is added
  5. customThe ethyl acetate layer is removed
  6. washwashed with water
  7. customdried
  8. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-3dc76b7cbf96470c94768566ceb196b9
Quelldatensatz
uspto-grants-1979_12
Patentnummer
US04179511

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