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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242490Generated: October 26, 2026

Methyl-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-amine → 2-Methyl-2-[4-({methyl-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-carbamoyl}-methyl)-phenoxy]-propionic acid tert-butyl ester

https://huagongshe.com/reaction/1242490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-amineHCID 21935732—
Reactant4-Carboxymethyl-phenoxy-2-methyl-propionic acid tert-butyl esterHCID 67072057—
Reactant[2-Methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-carbamic acid tert-butyl esterHCID 67072248—
Product2-Methyl-2-[4-({methyl-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-carbamoyl}-methyl)-phenoxy]-propionic acid tert-butyl esterHCID 69526544—

Reaction Steps

In analogy to the procedures described in example 26B] and 124C], methyl-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-amine (prepared from [2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-carbamic acid tert-butyl ester (example 125B] by N-methylation followed by Boc-cleavage in analogy to the procedures described in examples 5E] and 5F]) was reacted with 2-(4-carboxymethyl-phenoxy)-2-methyl-propionic acid tert-butyl ester (example 124A]) to give 2-methyl-2-[4-({methyl-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-carbamoyl}-methyl)-phenoxy]-propionic acid tert-butyl ester, which was subsequently cleaved with trifluoroacetic acid 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-31fb934902044d76898ed2124622393d
Source noteuspto-grants-2006_10