1,3-Diethyl 2-oxopropanedioate → Ethyl 5-chloro-2-oxo-1,2-dihydroquinoxaline-3-carboxylate

HRID 240354

Reaction equation

HRID 240354 reaction equation
[Cl:1][C:2]1[C:3]([NH2:9])=[C:4]([NH2:8])[CH:5]=[CH:6][CH:7]=1.O=[C:11]([C:17](OCC)=[O:18])[C:12]([O:14][CH2:15][CH3:16])=[O:13]>C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:3]=1[N:9]=[C:11]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:17](=[O:18])[NH:8]2

Participants

4

Reactant 2

HCID 691051,3-Diethyl 2-oxopropanedioateHCID 3462489(2-Amino-3-chlorophenyl)amine

Product 1

HCID 67531483Ethyl 5-chloro-2-oxo-1,2-dihydroquinoxaline-3-carboxylateYield 56.5%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent2×

Procedure

10.5 g (73.6 mmol) of 3-chloro-1,2-phenylenediamine and 12.8 g (73.5 mmol) of diethyl ketomalonate were dissolved in ethanol, and the solution was heated to reflux for 3 hours. While heating to reflux, ethanol was added thereto until precipitated crystals dissolved. The reaction mixture was cooled to room temperature, and then precipitated crystals were separated by filtration. The filter cake was washed with cold ethanol, and then dried, to obtain 10.5 g (yield: 51%) of ethyl 5-chloro-2-oxo-1,2-dihydroquinoxaline-3-carboxylate as pale yellow acicular crystals.

Workup

  1. temperaturethe solution was heated
  2. temperatureto reflux for 3 hours
  3. temperatureWhile heating
  4. temperatureto reflux
  5. customuntil precipitated crystals
  6. dissolutiondissolved
  7. customprecipitated crystals
  8. customwere separated by filtration
  9. washThe filter cake was washed with cold ethanol
  10. customdried

Sources & evidence

ORD record
ord-06d5eda75c2e4224b9590b1360ec3dbe
Source dataset
uspto-grants-2014_02
Patent number
US08648075B2

Linked notes

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