8-Hydroxy-2-quinolinecarboxaldehyde → HCID 178446986, compound
Reaction equation
[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([NH2:10])=[CH:9][C:4]=2[N:3]=[CH:2]1.[OH:11][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]2[C:21]=1[N:20]=[C:19]([CH:22]=O)[CH:18]=[CH:17]2.C([O:26][C:27](=O)[C:28](=[O:36])[CH2:29][C:30](=[O:35])[CH2:31][CH:32]([CH3:34])[CH3:33])C>C(O)C>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([N:10]3[CH:22]([C:19]4[CH:18]=[CH:17][C:16]5[C:21](=[C:12]([OH:11])[CH:13]=[CH:14][CH:15]=5)[N:20]=4)[C:29]([C:30](=[O:35])[CH2:31][CH:32]([CH3:34])[CH3:33])=[C:28]([OH:36])[C:27]3=[O:26])=[CH:9][C:4]=2[N:3]=[CH:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
1H-Benzoimidazol-5-ylamine (1 mmol) and 8-Hydroxy-quinoline-2-carbaldehyde (1 mmol) were added to ethanol (5 ml). After 30 min 6-Methyl-2,4-dioxo-heptanoic acid ethyl ester (1 mmol) was added. The reaction was heated to 50° C. and stirred for 24 h. After evaporation of the solvent the residue was purified with chromatographic methods.
Workup
- customAfter evaporation of the solvent the residue
- customwas purified with chromatographic methods
Sources & evidence
- ORD record
- ord-39ce91dfa05f448e8b62668caaa33045
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08278345B2
Reaction notes
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