Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424006Generated: October 30, 2026

2-Bromo-1-(3,3-dimethylpiperidin-1-yl)ethanone → 6-{2-{{4-[2-(3,3-Dimethylpiperidin-1-yl)ethoxy]-3-fluorobenzyl}methylamino}-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/2424006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(3,3-dimethylpiperidin-1-yl)ethanoneHCID 23363786—
ReactantPivalic acid 6-{2-[(3-fluoro-4-hydroxybenzoyl)methylamino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 66626888—
Product6-{2-{{4-[2-(3,3-Dimethylpiperidin-1-yl)ethoxy]-3-fluorobenzyl}methylamino}-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-olHCID 6662591950.9%

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-bromo-1-(3,3-dimethylpiperidin-1-yl)ethanone (19 mg) according to an analogous synthetic method to Example 404 and purified by LC-MS, the title compound (11 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-edc277e2c2ff49f78a04843badb034fa
Source noteuspto-grants-2011_06