Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075245Generated: November 1, 2026

HCID 131713046, compound → HCID 131713045, compound

https://huagongshe.com/reaction/1075245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131713046HCID 131713046—
SolventFormic AcidHCID 284—
ProductHCID 131713045HCID 13171304527.3%

Reaction Steps

A solution of 7-[2-allyloxyimino-2-(6-formamidopyridin-2-yl)acetamido]-3-(5-tert-butoxycarbonylaminomethyl-1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acid (syn isomer) (2.7 g) in formic acid (27 ml) was stirred for 2 hours at ambient temperature and evaporated to dryness. To the residue were added methanol (50 ml) and concentrated hydrochloric acid (0.82 g), and the mixture was stirred for an hour at ambient temperature. The solvent was evaporated and the residue was dissolved in water (50 ml), adjusted to pH 4 to 5 with an aqueous solution of sodium bicarbonate, treated with an activated charcoal and then subjected to column chromatography over nonionic adsorption resin, "Diaion HP 20" (80 ml). The column was washed with water and eluted with 50% aqueous methanol. The eluent containing a desired compound was evaporated to remove the methanol and then lyophilized to give 7-[2-allyloxyimino-2-(6-aminopyridin-2-yl)acetamido]-3-(5-aminomethyl-1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acid (syn isomer) (0.6 g), mp 180° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395411
Source datasetuspto-grants-1983_07
ORD IDord-8255b06e8af145f1835a7ba3f9782ae7
Source noteuspto-grants-1983_07