Potassium Nitrate → HCID 10588717, compound

HRID 1282295Notes

Reaction equation

HRID 1282295 reaction equation
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[NH:8][C:7](=[O:12])[C:6](=[O:13])[NH:5][C:4]=2[C:3]=1[C:14]([O:16][CH3:17])=[O:15].[N+:18]([O-])([O-:20])=[O:19].[K+]>OS(O)(=O)=O>[CH3:17][O:16][C:14]([C:3]1[C:4]2[NH:5][C:6](=[O:13])[C:7](=[O:12])[NH:8][C:9]=2[CH:10]=[C:11]([N+:18]([O-:20])=[O:19])[C:2]=1[CH3:1])=[O:15]

Participants

4

Reactant 2

HCID 24434Potassium NitrateHCID 10847279Methyl 1,2,3,4-tetrahydro-6-methyl-2,3-dioxo-5-quinoxalinecarboxylate

Product 1

HCID 10588717HCID 10588717, compound

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Procedure

To a solution of 6-methyl-2,3-dioxo- 1,2,3,4-tetrahydro-quinoxaline-5-carboxylic acid, methyl ester (1.11 g, 4.74 mmol) in conc. H2SO4 (15 mL) at room temperature was added in one portion with vigorous stirring potassium nitrate (0.529 g, 5.23 mmol). The reaction mixture was stirred for 23 hours and poured over ice. The precipitated product was thoroughly washed with water upon collection to give 1.28 g (97%).

Workup

  1. additionpoured over ice
  2. washThe precipitated product was thoroughly washed with water upon collection
  3. customto give 1.28 g (97%)

Sources & evidence

ORD record
ord-d6d81e580c7c4367b3edd88b66f64788
Source dataset
uspto-grants-2002_09
Patent number
US06455698B1

Reaction notes

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