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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68752Generated: October 26, 2026

3-Fluorophenylboronic acid → 1-(3-Fluoro-phenyl)-3-methylsulfanyl-6-(1,2,3,6-tetrahydro-pyridin-4-yl)-1H-indazole

https://huagongshe.com/reaction/68752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant4-(3-Methylsulfanyl-1H-indazol-6-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl esterHCID 67447024—
Product1-(3-Fluoro-phenyl)-3-methylsulfanyl-6-(1,2,3,6-tetrahydro-pyridin-4-yl)-1H-indazoleHCID 56666738—

Reaction Steps

The title compound was prepared as a white solid by coupling 4-(3-methylsulfanyl-1H-indazol-6-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester and 3-fluoro-phenyl boronic acid to yield an intermediate, which was de-protected to remove the N-Boc group.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822447B2
Source datasetuspto-grants-2014_09
ORD IDord-80a73feb29934c6eabc18cc191eb27c3
Source noteuspto-grants-2014_09