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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242494Generated: October 31, 2026

2-(4-Aminomethyl-phenoxy)-2-methyl-propionic acid ethyl ester → 2-Methyl-2-[4-({[4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl ester

https://huagongshe.com/reaction/1242494

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Aminomethyl-phenoxy)-2-methyl-propionic acid ethyl esterHCID 16109188—
Reactant4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acidHCID 21935767—
Reactant4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid ethyl esterHCID 86597809—
Product2-Methyl-2-[4-({[4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl esterHCID 86597818—

Reaction Steps

In analogy to the procedures described in example 26B] and 26C, 2-(4-aminomethyl-phenoxy)-2-methyl-propionic acid ethyl ester [PCT Int. Appl. (2002), WO 2002/096895A1] was reacted with 4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid (prepared by saponification from 4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid ethyl ester (example 107B]) in analogy to example 53B]) to give 2-methyl-2-[4-({[4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-9b313c060a474d9fbcd813c391a2cf26
Source noteuspto-grants-2006_10