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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184741Generated: November 2, 2026

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

https://huagongshe.com/reaction/1184741

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-(methylsulphonyl)benzeneboronic acidHCID 45933628—
Reactant4-(5-Chloro-2,3-dihydrofuro[2,3-c]pyridin-2-yl)piperidine-1-carboxylic acid tert-butyl esterHCID 86674895—
Product4-[5-(3-Fluoro-4-methanesulfonyl-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 67990232—

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 3-fluoro-4-(methanesulfonyl)phenylboronic acid acid following a procedure analogous to that described in Example 28. LC (method 10): tR=1.71 min; Mass spectrum (ESI+): m/z=477 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669271B2
Source datasetuspto-grants-2014_03
ORD IDord-0d987be3de3e468aafc89c8852b2948c
Source noteuspto-grants-2014_03