HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 131711006, compound → HCID 131711005, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 131711006 | HCID 131711006 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 131711005 | HCID 131711005 | — |
Reaction Steps
Each of the cis-and trans-isomers of tert-butyl 3-(2'-cyanovinyl)-7-phenoxyacetamido-3-cephem-4-carboxylate from Example 17 was in turn treated with 98-100 percent formic acid for 1 hour at room temperature to cleave the tert-butyl ester groups therefrom. After evaporation under reduced pressure of the excess formic acid, the acid residue was separated as an oil. Each product [the cis-or trans-isomer of the titled compound] showed a large antibiotic activity zone at 1 microgram/milliliter on a bioautograph test against B. subtilis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04065620 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-0ca60ff45d90461a9911be71d9fd5408 |
| Source note | uspto-grants-1977_12 |