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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434241Generated: October 27, 2026

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

https://huagongshe.com/reaction/1434241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-piperidine-1-yl-ethanoneHCID 222312—
ReactantPivalic acid 6-{2-[(3-fluoro-4-hydroxybenzoyl)methylamino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 66626888—
Product6-{2-{[3-Fluoro-4-(2-piperidin-1-ylethoxy)benzyl]methylamino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 6662637010.7%

Reaction Steps

Synthesized from pivalic acid 6-{2-[(3-fluoro-4-hydroxybenzoyl)methylamino]-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 (2.2 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-abf5035a9ec74c018a4f30dbfef0e570
Source noteuspto-grants-2009_11