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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423821Generated: October 29, 2026

HCID 23087193, compound → HCID 66627668, compound

https://huagongshe.com/reaction/2423821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23087193HCID 23087193—
Reactant3-Fluoro-4-(2-piperidin-1-ylethoxy)benzoic acid hydrochlorideHCID 66626827—
ReactantHCID 67242814HCID 67242814—
ProductHCID 66627668HCID 66627668—

Reaction Steps

Synthesized from 5-fluoro-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenylamine and 3-fluoro-4-(2-piperidin-1-ylethoxy)benzoic acid hydrochloride according to an analogous synthetic method to Example 282, [5-fluoro-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl][3-fluoro-4-(2-piperidin-1-ylethoxy)benzyl]amine (376 mg) was used according to an analogous synthetic method to Example 36 to provide ethyl[5-fluoro-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl][3-fluoro-4-(2-piperidin-1-ylethoxy)benzyl]amine (317 mg). This compound (315 mg) was used according to an analogous synthetic method to Example 111 to provide the title compound (265 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-6751eaff9dce4a09a6306bf31f2b9fcd
Source noteuspto-grants-2011_06