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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950139Generated: October 30, 2026

3-Fluoro-4-(2-piperidin-1-ylethoxy)benzoic acid hydrochloride → Ethyl[3-fluoro-4-(2-piperidin-1-ylethoxy)benzyl](5-methoxy-2-naphthalen-2-ylphenyl)amine

https://huagongshe.com/reaction/1950139

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-(2-piperidin-1-ylethoxy)benzoic acid hydrochlorideHCID 66626827—
Reactant[3-Fluoro-4-(2-piperidin-1-ylethoxy)benzyl](5-methoxy-2-naphthalen-2-ylphenyl)amineHCID 66627843—
ProductEthyl[3-fluoro-4-(2-piperidin-1-ylethoxy)benzyl](5-methoxy-2-naphthalen-2-ylphenyl)amineHCID 66627061—

Reaction Steps

Synthesized from 5-methoxy-2-naphthalen-2-ylamine and 3-fluoro-4-(2-piperidin-1-ylethoxy)benzoic acid hydrochloride according to an analogous synthetic method to Example 114, [3-fluoro-4-(2-piperidin-1-ylethoxy)benzyl](5-methoxy-2-naphthalen-2-ylphenyl)amine (290 mg) was used according to an analogous synthetic method to Example 36 to provide ethyl[3-fluoro-4-(2-piperidin-1-ylethoxy)benzyl](5-methoxy-2-naphthalen-2-ylphenyl)amine (252 mg). This compound (250 mg) was used according to an analogous synthetic method to Example 111 to provide the title compound (222 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399520B2
Source datasetuspto-grants-2013_03
ORD IDord-63f0f39423b64eff88a75a03c0f883df
Source noteuspto-grants-2013_03