HCID 12834157, compound → HCID 12834062, compound

HRID 1660609Notes

Reaction equation

HRID 1660609 reaction equation
[CH3:1][CH:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[N:5]2[C:11](=[O:33])[CH:12]([NH:13][C:14](=[O:32])[CH:15]([C:24]3[CH:29]=[CH:28][C:27]([S:30][CH3:31])=[CH:26][CH:25]=3)[NH:16]C(OC(C)(C)C)=O)[C@H:4]2[S:3]1>C(O)=O>[CH3:1][CH:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[N:5]2[C:11](=[O:33])[CH:12]([NH:13][C:14](=[O:32])[CH:15]([C:24]3[CH:29]=[CH:28][C:27]([S:30][CH3:31])=[CH:26][CH:25]=3)[NH2:16])[C@H:4]2[S:3]1

Participants

3

Procedure

A solution of 2-methyl-7-[N-(tert.-butoxycarbonyl)-2-(4-methylthiophenyl)glycyl]amino-3-cephem-4-carboxylic acid (3.0 g) in formic acid (100 ml) was stirred for 1 hour under anhydrous condition at room temperature. After the reaction was completed, the solvent was removed from the reaction mixture under reduced pressure, and the residue was dissolved in a mixture of water and ethyl acetate, after which the aqueous layer was separated. The aqueous layer was washed with ethyl acetate, and the organic solvent was completely removed under reduced pressure. The insoluble material was collected by filtration and lyophilized to give white powder of 2-methyl-7-[2-(4-methylthiophenyl)glycyl]amino-3-cephem-4-carboxylic acid (1.2 g), mp 165° to 175° C.

Workup

  1. customthe solvent was removed from the reaction mixture under reduced pressure
  2. dissolutionthe residue was dissolved in a mixture of water and ethyl acetate
  3. customafter which the aqueous layer was separated
  4. washThe aqueous layer was washed with ethyl acetate
  5. customthe organic solvent was completely removed under reduced pressure
  6. filtrationThe insoluble material was collected by filtration

Sources & evidence

ORD record
ord-954e655a9c6d42778eeaf23bdcee5999
Source dataset
uspto-grants-1981_12
Patent number
US04308380

Reaction notes

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