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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423980Generated: October 30, 2026

2-Chloro-1-(4-methylpiperidin-1-yl)ethan-1-one → 6-{2-{Ethyl {3-fluoro-4-[2-(4-methylpiperidin-1-yl)ethoxy]benzyl}amino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/2423980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-(4-methylpiperidin-1-yl)ethan-1-oneHCID 4116926—
ReactantPivalic acid 6-{2-[ethyl(3-fluoro-4-hydroxybenzoyl)amino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 57934183—
Product6-{2-{Ethyl {3-fluoro-4-[2-(4-methylpiperidin-1-yl)ethoxy]benzyl}amino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 5793397467.9%

Reaction Steps

Synthesized from pivalic acid 6-{2-[ethyl(3-fluoro-4-hydroxybenzoyl)amino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl ester (21 mg) and 2-chloro-1-(4-methylpiperidin-1-yl)ethanone (16 mg) according to an analogous synthetic method to Example 404 and purified by LC-MS, the title compound (15 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-d41b342e633a4d4f99127ac7720ad854
Source noteuspto-grants-2011_06