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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957114Generated: November 2, 2026

2-Butanamine, 2-methyl- → 6,7-dichloro-2,3-dimethoxy-5-{[2-(N-(1,1-dimethylpropyl)amino)ethyl]pyrazol-1-ylmethyl}quinoxaline

https://huagongshe.com/reaction/1957114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butanamine, 2-methyl-HCID 68986—
Reactant5-[(2-Chloroethyl)pyrazol-1-ylmethyl]-6,7-dichloro-2,3-dimethoxyquinoxalineHCID 54339196—
SolventEthanolHCID 702—
Product6,7-dichloro-2,3-dimethoxy-5-{[2-(N-(1,1-dimethylpropyl)amino)ethyl]pyrazol-1-ylmethyl}quinoxalineHCID 2322498838%

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of 5-[(2-chloroethyl)pyrazol-1-ylmethyl]-6,7-dichloro-2,3-dimethoxyquinoxaline (150 mg, 0.37 mmol), 1,1-dimethyl-1-propylamine (3 mL) and ethanol (5 mL) were heated in a closed vessel at 105° C. for 7 hours. The mixture was cooled, the solvent was removed under reduced pressure, and the residue was dissolved in ethyl acetate (75 mL). The solution was washed with saturated aqueous sodium bicarbonate, dried (MgSO4) and concentrated under reduced pressure. Purification by flash chromatography (elution with dichloromethane, then an ethyl acetate/methanol/triethylamine gradient) gave 6,7-dichloro-2,3-dimethoxy-5-{[2-(N-(1,1-dimethylpropyl)amino)ethyl]pyrazol-1-ylmethyl}quinoxaline (65 mg, 38%), as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783572
Source datasetuspto-grants-1998_07
ORD IDord-7e8695b6787e4c51a6b28f32700ac456
Source noteuspto-grants-1998_07