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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980980Generated: October 29, 2026

m-Chloroperbenzoic acid → HCID 131714356, compound

https://huagongshe.com/reaction/980980

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 131714357HCID 131714357—
SolventDichloromethaneHCID 6344—
ProductHCID 131714356HCID 13171435686.1%

Reaction Steps

To a solution of benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-[2-(3-pyridazinyl)vinyl]-2-cephem-4-carboxylate (syn isomer) (trans isomer) (2.1 g) in methylene chloride (40 ml) was added a solution of 70% m-chloroperbenzoic acid (0.87 g) in methylene chloride (20 ml) at -35° C. with stirring. The reaction mixture was stirred at the same temperature for 20 minutes. The resultant solution was washed with 5% aqueous sodium bicarbonate. The separated organic layer was concentrated under reduced pressure and the residue was triturated in diisopropyl ether to give benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-[2-(3-pyridazinyl)vinyl]-3-cephem-4-carboxylate-1-oxide (syn isomer) (trans isomer) (1.85 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04639448
Source datasetuspto-grants-1987_01
ORD IDord-0c6c83c98791481f82e6aed468879ecc
Source noteuspto-grants-1987_01