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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471799Generated: October 30, 2026

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

https://huagongshe.com/reaction/1471799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
Reactant4-(5-Chloro-furo[2,3-c]pyridin-2-yl)-4-methyl-piperidine-1-carboxylic acid tert-butyl esterHCID 86694576—
Product4-[5-(4-Methanesulfonyl-phenyl)-furo[2,3-c]pyridin-2-yl]-4-methyl-piperidine-1-carboxylic acid tert-butyl esterHCID 86694586—

Reaction Steps

The title compound is prepared from 4-(5-chloro-furo[2,3-c]pyridin-2-yl)-4-methyl-piperidine-1-carboxylic acid tert-butyl ester and 4-methanesulfonyl-phenylboronic acid following a procedure analogous to that described for Example 1; the reaction is conducted at 150° C. LC (method 4): tR=1.71 min; Mass spectrum (ESI+): m/z=471 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012456B2
Source datasetuspto-grants-2015_04
ORD IDord-1f0573f2643d4ef6bc38c20a34a694b3
Source noteuspto-grants-2015_04