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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434253Generated: November 1, 2026

2-Chloro-1-piperidine-1-yl-ethanone → 6-{4-Methoxy-2-{[4-(2-piperidin-1-ylethoxy)benzyl]propylamino}phenyl}-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/1434253

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-piperidine-1-yl-ethanoneHCID 222312—
ReactantPivalic acid 6-{2-[(4-hydroxybenzoyl)propylamino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 66626482—
Product6-{4-Methoxy-2-{[4-(2-piperidin-1-ylethoxy)benzyl]propylamino}phenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 6662560578%

Reaction Steps

Synthesized from pivalic acid 6-{2-[(4-hydroxybenzoyl)propylamino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl ester (30 mg) and 2-chloro-1-piperidin-1-ylethanone (19 mg) according to an analogous synthetic method to Example 404 and purified by LC-MS, the title compound (24 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-f3abd1e8c4854fb1a52973264cfe8375
Source noteuspto-grants-2009_11