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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242495Generated: October 30, 2026

4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid → 2-(4-{[4-Cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-ylcarbamoyl]-methyl}-phenoxy)-2-methyl-propionic acid tert-butyl ester

https://huagongshe.com/reaction/1242495

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acidHCID 21935767—
ReactantHCID 21935904HCID 21935904—
Reactant4-Carboxymethyl-phenoxy-2-methyl-propionic acid tert-butyl esterHCID 67072057—
Product2-(4-{[4-Cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-ylcarbamoyl]-methyl}-phenoxy)-2-methyl-propionic acid tert-butyl esterHCID 69525362—

Reaction Steps

In analogy to the procedures described in example 26B] and 124C], 4-cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-ylamine (prepared from 4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid, see example 133], in analogy to the procedures described in examples 125B] and 125C]) was reacted with 2-(4-carboxymethyl-phenoxy-2-methyl-propionic acid tert-butyl ester (example 124A]) to give 2-(4-{[4-cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-ylcarbamoyl]-methyl}-phenoxy)-2-methyl-propionic acid tert-butyl ester, which was subsequently cleaved with trifluoroacetic acid to yield the title compound as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-1a84e583ad08424597c81015a54c1694
Source noteuspto-grants-2006_10