Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423799Generated: October 30, 2026

4-(1-Acetylpiperidin-4-yloxy)benzaldehyde → (R)-6-{2-{Ethyl[4-(1-ethylpiperidin-4-yloxy)benzyl]amino}-4,5-dimethoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/2423799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-Acetylpiperidin-4-yloxy)benzaldehydeHCID 23087524—
Reactantpivalic acid (R)-6-(2-ethylamino-4,5-dimethoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 57934541—
Product(R)-6-{2-{Ethyl[4-(1-ethylpiperidin-4-yloxy)benzyl]amino}-4,5-dimethoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 5793426149.1%

Reaction Steps

Synthesized from pivalic acid (R)-6-(2-ethylamino-4,5-dimethoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-yl ester (20 mg) and 4-(1-acetylpiperidin-4-yloxy)benzaldehyde (57 mg) according to an analogous synthetic method to Example 264 and purified by LC-MS, the title compound (13 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-525c81913a814ab4b2cf06361f0ec8fb
Source noteuspto-grants-2011_06