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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184709Generated: October 25, 2026

2-Fluoro-4-(methylsulphonyl)benzeneboronic acid → 4-[5-Chloro-2-(2-fluoro-4-methanesulfonyl-phenyl)-pyridin-4-ylethynyl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1184709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-(methylsulphonyl)benzeneboronic acidHCID 44717666—
Reactant4-(2,5-Dichloro-pyridin-4-ylethynyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 86674893—
Product4-[5-Chloro-2-(2-fluoro-4-methanesulfonyl-phenyl)-pyridin-4-ylethynyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 67973679—

Reaction Steps

The title compound is prepared from 4-(2,5-dichloro-pyridin-4-ylethynyl)-piperidine-1-carboxylic acid tert-butyl ester and 2-fluoro-4-(methanesulfonyl)phenylboronic acid following a procedure analogous to that described for Intermediate 14. LC (method 7): tR=1.63 min; Mass spectrum (ESI+): m/z=493 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669271B2
Source datasetuspto-grants-2014_03
ORD IDord-3428c156c56045ea81ca51218eacd373
Source noteuspto-grants-2014_03