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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533132Generated: October 30, 2026

5-(2-Fluoro-4-methanesulfonylmethyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine → 5-(2-Fluoro-4-methanesulfonylmethyl-phenyl)-2-{1-[(1-trifluoromethyl-cyclopropyl)methyl]-piperidin-4-yl}-2,3-dihydrofuro[2,3-c]pyridine

https://huagongshe.com/reaction/533132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-Fluoro-4-methanesulfonylmethyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridineHCID 71208140—
Reactant(1-(Trifluoromethyl)cyclopropyl)methyl methanesulfonateHCID 86649942—
Product5-(2-Fluoro-4-methanesulfonylmethyl-phenyl)-2-{1-[(1-trifluoromethyl-cyclopropyl)methyl]-piperidin-4-yl}-2,3-dihydrofuro[2,3-c]pyridineHCID 71598654—

Reaction Steps

The title compound is prepared from 5-(2-fluoro-4-methanesulfonylmethyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and methanesulfonic acid (1-trifluoromethyl-cyclopropyl)methyl ester following a procedure analogous to that described for Example 2. LC (method 1): tR=1.01 min; Mass spectrum (ESI+): m/z=513 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853239B2
Source datasetuspto-grants-2014_10
ORD IDord-8e0c9373f31844059facf76dd904404a
Source noteuspto-grants-2014_10