Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 70468138 | HCID 70468138 | — |
| Reactant | HCID 178527944 | HCID 178527944 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14502354 | HCID 14502354 | 58% |
Reaction Steps
1.0 g. of 7-bromoacetamido-3-(2,6-dichlorobenzoylamino)methylceph-3-em-carboxylic acid and 0.36 g. of 2-phenyl-5-mercapto-1,3,4-oxadiazole were dissolved in 10 ml. of dimethyl formamide and 0.28 g. of calcinated potassium carbonate were added. The reaction mixture was stirred at room temperature for 8 hours, 30 ml. of ether were added, the precipitate was filtered off and dissolved in 30 ml. of water. The solution was adjusted to pH 5 by adding dilute sulphuric acid and extracted with 20 ml. of ethyl acetate. The aqueous layer was adjusted to pH 2 by adding dilute sulphuric acid and extracted with 60 ml. of ethyl acetate. The organic extract was dried over magnesium sulphate. The solvent was evaporated in vacuo and the residue was treated with ether and dried. 0.72 g. of 7-(2-phenyl-1,3,4-oxadiazole-5-ylthio)acetamido-3-(2,6-dichlorobenzoylamino)methylceph-3-em-4-carboxylic acid were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04626533 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-9b17ff1409e545dd90400b75a1299171 |
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| Source note | uspto-grants-1986_12 |
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