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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242474Generated: October 30, 2026

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

https://huagongshe.com/reaction/1242474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-methoxyacetoacetateHCID 123500—
Reactant2-(4-Aminomethyl-phenoxy)-2-methyl-propionic acid ethyl esterHCID 16109188—
Reactant4-Methoxymethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acidHCID 21935695—
Product2-[4-({[4-Methoxymethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-phenoxy]-2-methyl-propionic acid ethyl esterHCID 69667251—

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-methoxymethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid (prepared from 4-methoxy-3-oxo-butyric acid methyl ester, in analogy to the procedures described in examples 27C] and 27D] followed by saponification in analogy to the procedure described in example 53B]) to give 2-[4-({[4-methoxymethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-phenoxy]-2-methyl-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as light yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-d8e92e11aa94478b9c5edc376996b49a
Source noteuspto-grants-2006_10