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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269657Generated: October 30, 2026

Diisopropylethylamine → Ethyl [4-({butyl[6-(4-chlorophenyl)pyrazin-2-yl]amino}methyl)-2-methylphenoxy]acetate

https://huagongshe.com/reaction/1269657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Bromo-6-(4-chlorophenyl)pyrazineHCID 18448322—
ReactantEthyl {4-[(butylamino)methyl]-2-methylphenoxy}acetateHCID 58622846—
SolventDichloromethaneHCID 6344—
ProductEthyl [4-({butyl[6-(4-chlorophenyl)pyrazin-2-yl]amino}methyl)-2-methylphenoxy]acetateHCID 5862290016.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-bromo-6-(4-chlorophenyl)pyrazine (0.27 g, 1 mmol), N,N-diisopropylethylamine (0.18 mL, 1 mmol) and ethyl {4-[(butylamino)methyl]-2-methylphenoxy}acetate (0.42 g, 1.5 mmol) was heated at 100° C. in a sealed reactivial for 18 h. The reaction mixture was then allowed to come to room temperature and the residue dissolved in CH2Cl2 (50 mL), the organic extract was washed water (15 mL) and passed through a hydrophobic frit before concentrating in vacuo. Purification by Biotage™ chromatography (Si, 40 g) eluting 1:9–1:1.5 EtOAc:cyclohexane afforded the title compound as a pale yellow oil 78 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199239B2
Source datasetuspto-grants-2007_04
ORD IDord-c17837fa72f8446c9f6066e0af793a82
Source noteuspto-grants-2007_04