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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470208Generated: November 2, 2026

Water → Ceftobiprole

https://huagongshe.com/reaction/1470208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantHCID 90407255HCID 90407255—
ReactantHCID 178489948HCID 178489948—
Solventtert-Butyl methyl etherHCID 15413—
ProductCeftobiproleHCID 135413542—

Reaction Steps

A reactor is charged with (7R)-4-methoxybenzyl-3-((E)-((R)-1′-(tert-butoxycarbonyl)-2-oxo-[1,3′-bipyrrolidin]-3-ylidene)methyl)-7-((Z)-(2-hydroxybenzylidene)amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate (1 eq), water (6-9 weight % relative to the Schiff base), (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((4-methoxybenzyl)oxy)imino)acetic methanesulfonic anhydride (2.5 eq) and dichloromethane (1.75 mL per gram of Schiff base). The mixture is stirred for three hours at room temperature, then added to methyl tertiary butyl ether over the course of 2-3 hours, resulting in the formation of a solid. The solid is filtered and the filter cake was washed with additional methyl tertiary butyl ether. The filtered solid is deprotected using conventional methods and dried under vacuum to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006421B2
Source datasetuspto-grants-2015_04
ORD IDord-78c1381f904e41eb81fa106c2d13ae1e
Source noteuspto-grants-2015_04