Formic Acid → HCID 178517229, compound
Reaction equation
[NH2:1][C:2]1[C:11]([NH2:12])=[C:10]([Cl:13])[CH:9]=[C:8]2[C:3]=1[N:4]=[C:5]([OH:15])[C:6]([OH:14])=[N:7]2.[CH:16](O)=O>O>[Cl:13][C:10]1[CH:9]=[C:8]2[C:3]([N:4]=[C:5]([OH:15])[C:6]([OH:14])=[N:7]2)=[C:2]2[NH:1][CH:16]=[N:12][C:11]=12Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
A mixture of 0,3 g (1,35 mmol) 5,6-diamino-7-chloro-2,3-dihydroxyquinoxaline and 8 ml formic acid was refluxed for 2 h. After cooling to 25° C., the reaction mixture was poured into 30 ml water to give 0,21 g (67%) 4-chloro-7,8-dihydroxy-1H-imidazo(4,5-f)quinoxaline, m.p.>300° C. NMR (DMSO-d6): 7.37 (1H,s), 6.70 (1H,s).
Workup
- temperaturewas refluxed for 2 h
Sources & evidence
- ORD record
- ord-7fe556dfa07a408c84f4e6d05f694510
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05075306
Reaction notes
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