Potassium Hydroxide → HCID 68547606, compound
Reaction equation
[NH2:1][C:2]1[C:11]([C:12]([C:14]2[C:19]([O:20]C)=[CH:18][CH:17]=[CH:16][C:15]=2[O:22][CH3:23])=O)=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.O.NN.[OH-].[K+]>C(O)COCCO>[NH2:1][C:2]1[C:11]([CH2:12][C:14]2[C:15]([O:22][CH3:23])=[CH:16][CH:17]=[CH:18][C:19]=2[OH:20])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 160 °C
Procedure
(2-Aminoquinolin-3-yl)(2,6-dimethoxyphenyl)methanone (0.19 g, 0.6 mmol) was dissolved in diethylene glycol (10 mL), mixed with hydrazine hydrate (0.19 mL, 6.1 mmol) and pulverized potassium hydroxide (0.27 g, 6.7 mmol) and heated for 2 hours at 160° C. The same amounts of hydrazine hydrate and potassium hydroxide were added two more times and the reaction mixture was stirred for two more hours each time at 160° C.
Sources & evidence
- ORD record
- ord-713f64777da145abbf02804515a47ce6
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686002B2
Reaction notes
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