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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242411Generated: October 31, 2026

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

https://huagongshe.com/reaction/1242411

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-Cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetic acidHCID 21935630—
Reactant5-Chloromethyl-4-cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidineHCID 21935960—
Reactant2-Methyl-2-(3-methylamino-5-trifluoromethyl-phenoxy)-propionic acid ethyl esterHCID 67072310—
Product2-[3-({2-[4-Cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetyl}-methyl-amino)-5-trifluoromethyl-phenoxy)-2-methyl-propionic acid ethyl esterHCID 86597807—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-d35e2d7750904f7b95da0c591e9713b1
Source noteuspto-grants-2006_10