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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471774Generated: October 25, 2026

3-Fluoro-4-(methylsulphonyl)benzeneboronic acid → 4-[5-(3-Fluoro-4-methanesulfonyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1471774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-(methylsulphonyl)benzeneboronic acidHCID 45933628—
Reactant4-(5-Chlorofuro[2,3-c]pyridin-2-yl)piperidine-1-carboxylic acid tert-butyl esterHCID 86674889—
Product4-[5-(3-Fluoro-4-methanesulfonyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 71736412—

Reaction Steps

The title compound is prepared from 4-(5-chloro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester and 3-fluoro-4-methylsulfonyl-phenylboronic acid following a procedure analogous to that described for Example 1. LC (method 4): tR=1.71 min; Mass spectrum (ESI+): m/z=475 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012456B2
Source datasetuspto-grants-2015_04
ORD IDord-2f3f2234eba54102847af007a150eabd
Source noteuspto-grants-2015_04