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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269668Generated: November 1, 2026

Diisopropylethylamine → Ethyl [4-({butyl[5-methyl-6-(4-methylphenyl)pyrimidin-4-yl]amino}methyl)-2-ethylphenoxy]acetate

https://huagongshe.com/reaction/1269668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-5-methyl-6-(4-methylphenyl)pyrimidineHCID 18448402—
ReactantEthyl {4-[(butylamino)methyl]-2-ethylphenoxy}acetateHCID 58622897—
SolventDichloromethaneHCID 6344—
ProductEthyl [4-({butyl[5-methyl-6-(4-methylphenyl)pyrimidin-4-yl]amino}methyl)-2-ethylphenoxy]acetateHCID 5862284318.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl {4-[(butylamino)methyl]-2-ethylphenoxy}acetate (0.23 g, 0.78 mmol), N,N-diisopropylethylamine (0.18 mL, 1.05 mmol) and 4-chloro-5-methyl-6-(4-methylphenyl)pyrimidine (0.114 g, 0.52 mmol) were heated at 100° C. in a sealed reactivial for 18 h. After this time the reactivial was allowed to cool to room temperature and the residue dissolved in CH2Cl2 (50 mL) and washed with water (10 mL) and brine (10 mL). The organic extract was separated by hydrophobic frit and evaporated. Purification by Biotage™ chromatography (Silica, 40 g) eluting 9:1 cyclohexane:EtOAc afforded the title compound as a pale yellow oil (46 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199239B2
Source datasetuspto-grants-2007_04
ORD IDord-56677ac0fd02454c999dd14387ff9aea
Source noteuspto-grants-2007_04