Water → Tert-butyl 7-amino-3-methoxymethyl-3-cephem-4-carboxylate

HRID 1463090Notes

Reaction equation

HRID 1463090 reaction equation
S(C1C=CC(C)=CC=1)(O)(=O)=O.[NH2:12][CH:13]1[C:30](=[O:31])[N:15]2[C:16]([C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])=[C:17]([CH2:20][O:21][CH3:22])[CH2:18][S:19][C@H:14]12.O.C(=O)(O)[O-].[Na+]>C(Cl)Cl>[NH2:12][CH:13]1[C:30](=[O:31])[N:15]2[C:16]([C:23]([O:25][C:26]([CH3:27])([CH3:28])[CH3:29])=[O:24])=[C:17]([CH2:20][O:21][CH3:22])[CH2:18][S:19][C@H:14]12

Participants

5

Procedure

To a suspension of tert-butyl 7-amino-3-methoxymethyl-3-cephem-4-carboxylate tosylate (13.1 g) in methylene chloride (200 ml) was added water (100 ml), followed by adjusting to pH about 6 with an aqueous solution of sodium bicarbonate. After separating out the methylene chloride layer, the remaining aqueous solution was extracted with methylene chloride (50 ml). The combined methylene chloride solution was washed with an aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and then treated with an activated charcoal, followed by evaporation under reduced pressure to give tert-butyl 7-amino-3-methoxymethyl-3-cephem-4-carboxylate (5.7 g).

Workup

  1. customAfter separating out the methylene chloride layer
  2. extractionthe remaining aqueous solution was extracted with methylene chloride (50 ml)
  3. washThe combined methylene chloride solution was washed with an aqueous solution of sodium chloride
  4. dry with materialdried over anhydrous magnesium sulfate
  5. additiontreated with an activated charcoal
  6. customfollowed by evaporation under reduced pressure

Sources & evidence

ORD record
ord-3bb8687ebcab44d0a254a8549e95a934
Source dataset
uspto-grants-1984_07
Patent number
US04462999

Reaction notes

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