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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568244Generated: October 30, 2026

2-Fluoroethyl trifluoromethanesulfonate → HCID 178459458, compound

https://huagongshe.com/reaction/568244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoroethyl trifluoromethanesulfonateHCID 13638935—
ReactantHCID 131722333HCID 131722333—
ProductHCID 178459458HCID 17845945898.1%

Reaction Steps

2-Fluoroethyl trifluoromethanesulfonate (76.4 mg) is added to 41.1 mg of allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-(imidazo[5,1-b]thiazol-2-yl)methylpyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate described in Example 23-a), and the mixture is stirred in an argon atmosphere at room temperature for 2 hr. The solvent is removed by evaporation under reduced pressure, and the residue is purified by column chromatography on Sephadex LH-20 (dichloromethane:methanol 1:1) to give 54.1 mg of allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-[6-(2-fluoroethyl)imidazo[5,1-b]thiazolium-2-yl]methylpyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate trifluoromethanesulfonate as a yellow viscous material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180622B2
Source datasetuspto-grants-2001_01
ORD IDord-243e3d2047bb450cbd5c3fc83f484dee
Source noteuspto-grants-2001_01