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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533127Generated: October 29, 2026

4-(Methanesulfonyl)phenylboronic acid → (R)-4-[5-(4-Methanesulfonyl-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/533127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
Reactant(R)-4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 86675682—
Product(R)-4-[5-(4-Methanesulfonyl-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 71208264—

Reaction Steps

The title compound is prepared from (R)-4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester and 4-(methanesulfonyl)phenylboronic acid following a procedure analogous to that described for Intermediate 10. LC (method 1): tR=1.68 min; Mass spectrum (ESI+): m/z=459 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853239B2
Source datasetuspto-grants-2014_10
ORD IDord-27b0dd39145b4d74ade24e534da31e95
Source noteuspto-grants-2014_10