Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434022Generated: November 1, 2026

4-(4-Carboxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester → 6-{2-{Ethyl[4-(1-methylpiperidin-4-yl)benzyl]amino}-5-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/1434022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Carboxy-phenyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 22492859—
ReactantPivalic acid 6-(2-ethylamino-5-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 57934366—
Product6-{2-{Ethyl[4-(1-methylpiperidin-4-yl)benzyl]amino}-5-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 5793452178.7%

Reaction Steps

Synthesized from pivalic acid 6-(2-ethylamino-5-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-yl ester (50 mg) and 4-(4-carboxyphenyl)piperidine-1-carboxylic acid tert-butyl ester (100 mg) according to an analogous synthetic method to Example 337 described below, the title compound (50 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-9a6224f031904ff0ad11d0d7fb325894
Source noteuspto-grants-2009_11