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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5524Generated: October 29, 2026

Formic Acid → HCID 131718127, compound

https://huagongshe.com/reaction/5524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131718129HCID 131718129—
SolventEthyl AcetateHCID 8857—
ProductHCID 131718127HCID 13171812733%

Reaction Steps

To a mixture of formic acid (10 ml) and trifluoroacetic acid (5 ml) was added 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-(1-methyl-4-tert-butoxycarbonyl-1-piperazinio)methyl-3-cephem-4-carboxylate hydrochloride (syn isomer) (5.7 g) at 20° C. under stirring. The stirring was continued for 1.5 hours at the same temperature. The reaction mixture was poured into ethyl acetate (200 ml). The resulting precipietes were collected by filtration, added to water. The mixture was adjusted to pH 2.0 with a saturated aqueous solution of sodium bicarbonate and filtered. The filtrate was subjected to column chromatography on Diaion HP-20 using 10% aqueous isopropanol as an eluent. The eluate was evaporated in vacuo to remove isopropanol and then lyophilized to give 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-(1-methyl-1-piperazinio)methyl-3-cephem-4-carboxylate (syn isomer) (1.50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244890
Source datasetuspto-grants-1993_09
ORD IDord-cc6c87b9be304b508b4408d695432fd7
Source noteuspto-grants-1993_09