Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471784Generated: October 30, 2026

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

https://huagongshe.com/reaction/1471784

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(Methylsulfonyl)methyl]phenylboronic acidHCID 3746819—
Reactant4-(5-Chlorofuro[2,3-c]pyridin-2-yl)piperidine-1-carboxylic acid tert-butyl esterHCID 86674889—
Product4-[5-(4-Methanesulfonylmethyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 71736573—

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 4-methylsulfonylmethyl-phenylboronic acid following a procedure analogous to that described for Example 1; the reaction is conducted at 150° C. LC (method 1): tR=1.26 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-0c789e9251d34e34a3a647becbf8f354
Source noteuspto-grants-2015_04