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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533121Generated: October 25, 2026

4-[(Methylsulfonyl)methyl]phenylboronic acid → 4-[5-(4-Methanesulfonylmethylphenyl)-2,3-dihydrofuro[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/533121

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(Methylsulfonyl)methyl]phenylboronic acidHCID 3746819—
Reactant4-(5-Chloro-2,3-dihydrofuro[2,3-c]pyridin-2-yl)piperidine-1-carboxylic acid tert-butyl esterHCID 86674895—
Product4-[5-(4-Methanesulfonylmethylphenyl)-2,3-dihydrofuro[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 57389307—

Reaction Steps

The title compound is prepared from 4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester and 4-(methanesulfonylmethyl)phenyl boronic acid following a procedure analogous to that described for Intermediate 10. LC (method 1): tR=1.55 min; Mass spectrum (ESI+): m/z=473 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853239B2
Source datasetuspto-grants-2014_10
ORD IDord-7d16b73750244c39a2aefcad2be9641c
Source noteuspto-grants-2014_10