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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366110Generated: November 1, 2026

Acetic Acid → N-(2-(7-bromo-3-(4-methoxyphenyl)-2-oxoquinoxalin-1(2H)-yl)ethyl)acetamide

https://huagongshe.com/reaction/1366110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl 2-(4-methoxyphenyl)-2-oxoacetateHCID 2758864—
ReactantN-(2-(2-amino-5-bromophenylamino)ethyl)acetamideHCID 59822530—
SolventEthanolHCID 702—
ProductN-(2-(7-bromo-3-(4-methoxyphenyl)-2-oxoquinoxalin-1(2H)-yl)ethyl)acetamideHCID 59822532—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of crude N-(2-(2-amino-5-bromophenylamino)ethyl)acetamide from Example 14 in ethanol (0.74 mL) 870 mg of ethyl 2-(4-methoxyphenyl)-2-oxoacetate was added. To that mixture acetic acid was added resulting in of 1% v/v AcOH in EtOH solution. The reaction mixture was stirred at 80° C. for 18 h and allowed to cool to room temperature. The yellow precipitate was collected by filtration and washed with two 5 mL portions of EtOH. The yellow solid was dried under vacuum to provide N-(2-(7-bromo-3-(4-methoxyphenyl)-2-oxoquinoxalin-1(2H)-yl)ethyl)acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893066B2
Source datasetuspto-grants-2011_02
ORD IDord-61fe8b2a9b254304a88624f598e50811
Source noteuspto-grants-2011_02