HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131711626, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-((4-Methylphenyl)sulfonyl)-1H-isoindole-1,3(2H)-dione | HCID 214133 | — |
| Reactant | Desacetylcephalothin sodium | HCID 23695995 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131711626 | HCID 131711626 | 58.5% |
Reaction Steps
In N,N-dimethylformamide (40 ml) is dissolved in 7β-(2-thienylacetamido)-3-hydroxymethyl-3-cephem-4-carboxylic acid sodium salt (3.8 g), followed by the addition of N-tosylphthalimide (4.0 g) and triethylamine (2.0 ml) in that order. The mixture is stirred at room temperature for 4 hours. The reaction mixture is poured in water (100 ml) and rinsed with ethyl acetate. The aqueous layer is adjusted to pH 2.0 with dilute phosphoric acid and extracted with ethyl acetate. The extract is dried and, then, a solution of sodium 2-ethylhexanoate in isopropyl alcohol is added. By this procedure is obtained 7β-(2-thienylacetamido)-3-[2-(N-tosylcarbamoyl) benzoyloxy]methyl-3-cephem-4-carboxylic acid sodium salt (4.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04224441 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-5bf41c9eee674cbeb5ae848a5e81ec75 |
| Source note | uspto-grants-1980_09 |