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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242493Generated: October 27, 2026

2-(4-Aminomethyl-phenoxy)-2-methyl-propionic acid ethyl ester → 2-Methyl-2-[4-({[4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyridine-3-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl ester

https://huagongshe.com/reaction/1242493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Aminomethyl-phenoxy)-2-methyl-propionic acid ethyl esterHCID 16109188—
Reactant4-Trifluoromethyl-6-(4-trifluoromethyl-phenyl)-nicotinic acidHCID 21935758—
Reactant3-Pyridinecarboxylic acid,4-(trifluoromethyl)-6-[4-(trifluoromethyl)phenyl]-,methyl esterHCID 76852878—
Product2-Methyl-2-[4-({[4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyridine-3-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl esterHCID 86597817—

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-6-(4-trifluoromethyl-phenyl)-nicotinic acid (prepared from 4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-nicotinic acid methyl ester (example 108B]) by saponification in analogy to example 53B]) to give 2-methyl-2-[4-({[4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyridine-3-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as amorphous light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-74b1ab2bb6d14c5abaa5a3a79556d3f1
Source noteuspto-grants-2006_10