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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423707Generated: October 30, 2026

1-(2-(4-Bromo-2-fluorophenoxy)ethyl)piperidine → 3-[3-Fluoro-4-(2-piperidin-1-ylethoxy)phenylamino]-4-naphthalen-2-ylphenol

https://huagongshe.com/reaction/2423707

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-(4-Bromo-2-fluorophenoxy)ethyl)piperidineHCID 23087072—
Reactant[3-Fluoro-4-(2-piperidin-1-ylethoxy)phenyl](5-methoxy-2-naphthalen-2-ylphenyl)amineHCID 66625495—
Product3-[3-Fluoro-4-(2-piperidin-1-ylethoxy)phenylamino]-4-naphthalen-2-ylphenolHCID 5793426986.3%

Reaction Steps

Synthesized from 5-methoxy-2-naphthalen-2-ylamine and 1-[2-(4-bromo-2-fluorophenoxy)ethyl]piperidine according to an analogous synthetic method to Example 116, [3-fluoro-4-(2-piperidin-1-ylethoxy)phenyl](5-methoxy-2-naphthalen-2-ylphenyl)amine (350 mg) was used according to an analogous synthetic method to Example 111 to provide the title compound (293 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-478a2eb5c3ec4edbadfdf5c21ace1519
Source noteuspto-grants-2011_06