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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005863Generated: October 25, 2026

4-[5-(4-Fluorophenyl)pyridin-2-yl]piperazine dihydrochloride → 4-(R)-Benzyl-3-(2-(R)-{4-[5-(4-fluorophenyl)pyridin-2-yl]piperazine-1-sulfonylmethyl}-3-methylbutyryl)-oxazolidin-2-one

https://huagongshe.com/reaction/1005863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[5-(4-Fluorophenyl)pyridin-2-yl]piperazine dihydrochlorideHCID 22646693—
Reactant4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3 methylbutyryl)oxazolidin-2-oneHCID 22888284—
Reactant2-[4-(4-Bromo-phenyl)piperazine-1-sulfonylmethyl]3-methylbutyric acid tert-butyl esterHCID 69895250—
Product4-(R)-Benzyl-3-(2-(R)-{4-[5-(4-fluorophenyl)pyridin-2-yl]piperazine-1-sulfonylmethyl}-3-methylbutyryl)-oxazolidin-2-oneHCID 2351975385.9%

Reaction Steps

Prepared according to the method for the preparation of 2-[4-(4-bromophenyl)-piperazine-1-sulfonylmethyl]-3-methyl-butyric acid tert-butyl ester, from 4-[5-(4-fluorophenyl)pyridin-2-yl]piperazine dihydrochloride (0.108 g) and 4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3-methylbutyryl)oxazolidin-2-one (0.147 g), to yield the title compound as a pale green gum (0.167 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787536B2
Source datasetuspto-grants-2004_09
ORD IDord-594f815d65204e579839beddcc42c13f
Source noteuspto-grants-2004_09