HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462317Generated: October 30, 2026
HCID 131711009, compound → HCID 131711008, compound
https://huagongshe.com/reaction/462317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 131711009 | HCID 131711009 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 131711008 | HCID 131711008 | — |
Reaction Steps
A solution of 25 mg. of tert-butyl 7-(2'-tert-butoxycarbonylamino-2'-phenylacetamido)-3-(2'-tert-butoxycarbonylvinyl)-3-cephem-4-carboxylate, prepared as described in Example 19, in 5 cc of 98-100 percent formic acid was allowed to stand for 1 hour at room temperature. After evaporating under reduced pressure the formic acid, the acid residue was taken up in trifluoroacetic acid and the NMR spectrum was taken. The trifluoroacetic acid was removed under reduced pressure and the acid residue showed a β-lactam in the IR spectrum and an acceptable UV [λ max.=317 mμ (ε = 13,700)]. The bioautograph showed only one antibiotically active zone against Sarcina lutea, which was more polar than cephalexin. Disc plate assay procedures showed antibiotic activity against a variety of Gram positive and Gram negative microorganisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04065620 |
|---|
| Source dataset | uspto-grants-1977_12 |
|---|
| ORD ID | ord-fdc0860afd134bc9bbcb01429333b6d9 |
|---|
| Source note | uspto-grants-1977_12 |
|---|