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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462317Generated: October 30, 2026

HCID 131711009, compound → HCID 131711008, compound

https://huagongshe.com/reaction/462317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131711009HCID 131711009—
SolventFormic AcidHCID 284—
ProductHCID 131711008HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04065620
Source datasetuspto-grants-1977_12
ORD IDord-fdc0860afd134bc9bbcb01429333b6d9
Source noteuspto-grants-1977_12