Reaction equation
[Cl:1][C:2]1[C:7]2[C:8](=O)[O:9][CH:10](O)[C:6]=2[CH:5]=[C:4]([Cl:13])[N:3]=1.S(O)(O)(=O)=O.[NH2:19][NH2:20].C([O-])(=O)C.[Na+]>O>[Cl:1][C:2]1[C:7]2[C:8](=[O:9])[NH:19][N:20]=[CH:10][C:6]=2[CH:5]=[C:4]([Cl:13])[N:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 4,6-dichloro-1-hydroxy-1H-furo[3,4-c]pyridin-3-one (9.37 g) stirring in water (100 ml) was added hydrazine sulfate (10.58 ml) and sodium acetate (13.56 g). The reaction mixture was heated at reflux and stirred for 2 h. The reaction mixture was cooled to RT, diluted with water (150 ml) and extracted with EtOAc (2×75 ml). The combined organic layers were washed with saturated Na2CO3 solution and dried over Na2SO4. Evaporation to dryness gave the desired product as brown solid.
Workup
- temperatureThe reaction mixture was heated
- temperatureat reflux
- extractionextracted with EtOAc (2×75 ml)
- washThe combined organic layers were washed with saturated Na2CO3 solution
- dry with materialdried over Na2SO4
- customEvaporation to dryness
Sources & evidence
- ORD record
- ord-8c9942035d80453ba2ad8fdc7f24cb17
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09315500B2
Linked notes
Loading…