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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950522Generated: November 2, 2026

2-Chloro-1-piperidine-1-yl-ethanone → (S)-6-{2-{Ethyl[3-fluoro-4-(2-piperidin-1-ylethoxy)benzyl]amino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/1950522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-piperidine-1-yl-ethanoneHCID 222312—
ReactantHCID 57934250HCID 57934250—
Product(S)-6-{2-{Ethyl[3-fluoro-4-(2-piperidin-1-ylethoxy)benzyl]amino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 579337733.9%

Reaction Steps

Synthesized from pivalic acid (S)-6-{2-[ethyl(3-fluoro-4-hydroxybenzoyl)amino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl ester (20 mg) and 2-chloro-1-piperidin-1-ylethanone (13 mg) according to an analogous synthetic method to Example 404 and purified by LC-MS, the title compound (0.8 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399520B2
Source datasetuspto-grants-2013_03
ORD IDord-efb3ba71c1444c5190aa4196a9cf9e90
Source noteuspto-grants-2013_03