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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242383Generated: October 30, 2026

Ethyl 3-oxoheptanoate → 2-[3-({2-[4-Butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetyl}-methyl-amino)-phenoxy]-2-methyl-propionic acid ethyl ester

https://huagongshe.com/reaction/1242383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-oxoheptanoateHCID 559036—
Reactant[4-Butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetic acidHCID 21935713—
Reactant2-Methyl-2-(3-methylamino-phenoxy)-propionic acid ethyl esterHCID 67072118—
Product2-[3-({2-[4-Butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetyl}-methyl-amino)-phenoxy]-2-methyl-propionic acid ethyl esterHCID 67072397—

Reaction Steps

In analogy to the procedures described in example 26B] and 26C], 2-methyl-2-(3-methylamino-phenoxy)-propionic acid ethyl ester (example 26 A]) was reacted with [4-butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetic acid (prepared starting from 3-oxo-heptanoic acid ethyl ester in analogy to the sequences described in examples 27C] to 27F] and examples 26D] and 26E]) to give 2-[3-({2-[4-butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetyl}-methyl-amino)-phenoxy]-2-methyl-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as light yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-ee3e5fda1f014b38aa53672edc108e89
Source noteuspto-grants-2006_10