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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005869Generated: October 26, 2026

5-(4-Fluorophenyl)-2-(piperidin-4-yloxy)pyridine → 4-(R)-Benzyl-3-(2-(R)-{4-[5-(4-fluorophenyl)pyridin-2-yloxy]piperidine-1-sulfonylmethyl}-3-methylbutyryl)-oxazolidin-2-one

https://huagongshe.com/reaction/1005869

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Fluorophenyl)-2-(piperidin-4-yloxy)pyridineHCID 22646730—
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-yloxy]piperidine-1-sulfonylmethyl}-3-methylbutyryl)-oxazolidin-2-oneHCID 2351975275.3%

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 5-(4-fluorophenyl)-2-(piperidin-4-yloxy)pyridine (0.52 g) and 4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3-methylbutyryl)oxazolidin-2-one (0.57 g) to yield the title compound as an off-white solid (0.70 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787536B2
Source datasetuspto-grants-2004_09
ORD IDord-972250f74e684585a7824d46ce6c53a1
Source noteuspto-grants-2004_09