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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl 2-(4-methoxyphenyl)-2-oxoacetate | HCID 2758864 | — |
| Reactant | N-(2-(2-amino-5-bromophenylamino)ethyl)acetamide | HCID 59822530 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-(7-bromo-3-(4-methoxyphenyl)-2-oxoquinoxalin-1(2H)-yl)ethyl)acetamide | HCID 59822532 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893066B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-61fe8b2a9b254304a88624f598e50811 |
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| Source note | uspto-grants-2011_02 |
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