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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424109Generated: November 3, 2026

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

https://huagongshe.com/reaction/2424109

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-(4-methylpiperidin-1-yl)ethan-1-oneHCID 4116926—
ReactantPivalic acid (R)-6-{2-[ethyl(4-hydroxybenzoyl)amino]-4,5-dimethoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 57934042—
Product(R)-6-{2-{Ethyl {4-[2-(4-methylpiperidin-1-yl)ethoxy]benzyl}amino}-4,5-dimethoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 5802308941%

Reaction Steps

Synthesized from pivalic acid (R)-6-{2-[ethyl(4-hydroxybenzoyl)amino]-4,5-dimethoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl ester (16 mg) and 2-chloro-1-(4-methylpiperidin-1-yl)ethanone (9.5 mg) according to an analogous synthetic method to Example 404 and purified by LC-MS, the title compound (6.9 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-2d99696acb6a4ce1b4504b54c355c88f
Source noteuspto-grants-2011_06