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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242431Generated: October 31, 2026

Methyl 5-methoxy-3-oxopentanoate → HCID 67072257, compound

https://huagongshe.com/reaction/1242431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-methoxy-3-oxopentanoateHCID 542416—
Reactant4-(2-Methoxy-ethyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acidHCID 21935638—
ReactantHCID 23563108HCID 23563108—
ProductHCID 67072257HCID 67072257—

Reaction Steps

In analogy to the procedures described in example 26B] and 26C], 2-(4-aminomethyl-2-methyl-phenoxy)-2-methyl-propionic acid ethyl ester (example 97B]) was reacted with 4-(2-methoxy-ethyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid (prepared from 5-methoxy-3-oxo-pentanoic 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-(2-methoxy-ethyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-2-methyl-phenoxy]-2-methyl-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-c125e180395648f99924e13da1d1b9bd
Source noteuspto-grants-2006_10