HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131714355, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 131714353 | HCID 131714353 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131714355 | HCID 131714355 | 82.7% |
Reaction Steps
A solution of benzhydryl 7-[2-(2-formamidothiazol-4-yl)-2-methoxyiminoacetamido]-3-formyl-3-cephem-4-carboxylate (syn isomer) (3 g) and triethylamine (0.45 g) in tetrahydrofuran (30 ml) was stirred at ambient temperature for 40 minutes. To the reaction mixture was added ethyl acetate (50 ml) and washed with 3% hydrochloric acid and brine. The organic solution was dried over magnesium sulfate and evaporated. The residue was pulverized in diisopropyl ether to give benzhydryl 7-[2-(2-formamidothiazol-4-yl)-2-methoxyiminoacetamido]-3-formyl-2-cephem-4-carboxylate (syn isomer) (2.48 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04546101 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-24f9b76225da447d93acb511ffacae9e |
| Source note | uspto-grants-1985_10 |