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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533131Generated: October 29, 2026

5-(1-Methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydrofuro[2,3-c]pyridine → 5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-{1-[(1-trifluoromethyl-cyclopropyl)methyl]-piperidin-4-yl}-2,3-dihydro-furo[2,3-c]pyridine

https://huagongshe.com/reaction/533131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(1-Methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydrofuro[2,3-c]pyridineHCID 67973503—
Reactant(1-(Trifluoromethyl)cyclopropyl)methyl methanesulfonateHCID 86649942—
Product5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-{1-[(1-trifluoromethyl-cyclopropyl)methyl]-piperidin-4-yl}-2,3-dihydro-furo[2,3-c]pyridineHCID 71598653—

Reaction Steps

The title compound is prepared from 5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-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 3): tR=0.67 min; Mass spectrum (ESI+): m/z=486 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853239B2
Source datasetuspto-grants-2014_10
ORD IDord-64a3a0e5c372493c98a024a3c3e9d90f
Source noteuspto-grants-2014_10