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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242378Generated: October 30, 2026

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

https://huagongshe.com/reaction/1242378

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-6-(4-trifluoromethyl-phenyl)-nicotinic acidHCID 21935885—
Reactant2-Methyl-6-(4-trifluoromethyl-phenyl)-nicotinic Acid Methyl EsterHCID 67072269—
Reactant2-Methyl-2-(3-methylaminomethyl-phenoxy)-propionic acid ethyl esterHCID 67072273—
Product2-Methyl-2-[3-({methyl-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine-3-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl esterHCID 67072012—

Reaction Steps

In analogy to the procedures described in example 26B] and 26C], 2-methyl-2-(3-methylaminomethyl-phenoxy)-propionic acid ethyl ester (example 52C]) was reacted with 2-methyl-6-(4-trifluoromethyl-phenyl)-nicotinic acid (prepared from 2-methyl-6-(4-trifluoromethyl-phenyl)-nicotinic acid methyl ester (example 1L]) in analogy to the procedure described in example 53B]) to give 2-methyl-2-[3-({methyl-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine-3-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-f8b436ec3cee417c9ce6d2e9b61b3375
Source noteuspto-grants-2006_10