Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792623Generated: November 4, 2026

6-Bromo-4-{4-[4-(methylsulfonyl)phenoxy]piperidino}quinoline → 4-[4-(4-methylsulfonylphenoxy)piperidin-1-yl]-6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl) quinoline

https://huagongshe.com/reaction/1792623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-4-{4-[4-(methylsulfonyl)phenoxy]piperidino}quinolineHCID 22031182—
Reactant[3-(Trifluoromethyl)-1-trityl-1H-pyrazol-4-YL]boronic acidHCID 22032227—
Product4-[4-(4-methylsulfonylphenoxy)piperidin-1-yl]-6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl) quinolineHCID 6881406898.9%

Reaction Steps

150 mg 6-bromo-4-{4-[4-(methylsulfonyl)phenoxy]piperidino}quinoline (compound in Production Example 89) and 180 mg 3-trifluoromethyl-1-trityl-1H-4-pyrazolylboronic acid (compound in Production Example 31) were reacted in the same manner as in Example 9, to give 244 mg 4-[4-(4-methylsulfonylphenoxy)piperidin-1-yl]-6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl) quinoline. This product was reacted in the same manner as in Example 67, to give 130 mg of the title compound as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074801B1
Source datasetuspto-grants-2006_07
ORD IDord-d3ecdb12e6c848a6abe3d00d7327c16f
Source noteuspto-grants-2006_07