Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | 3-Bromo-4,5-dimethoxybenzaldehyde | HCID 81379 | — |
| Reactant | 2-Amino-8-quinolinol | HCID 4653788 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69093549 | HCID 69093549 | — |
Reaction Steps
2-Amino-8-hydroxyquinoline (192 mg, 1.2 mmol), 3-bromo-4,5-dimethoxy-benzaldehyde (245 mg, 1 mmol) and malononitrile (66 mg, 1 mmol) were suspended in 25 ml ethanol at room temperature, charged with DABCO (33 μl, 0.3 mmol) and then stirred at 90° C. under LC-MS control for 6 days. The desired product was formed as a main component with some side products and a small amount of starting material was left. The reaction mixture was cooled down to room temperature, diluted with water to about 100 ml and stirred for over night at room temperature. Thus resulting precipitates were collected by filtration, washed well with 1:1 mixture of ethanol/water and finally with small portion of 10% ethyl acetate in cyclohexane and then dried under high vacuum to get pure solids (202 mg, 0.45 mmol, 45%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371333B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-3f30ecb7cba346be8f2466d3bada9c2e |
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| Source note | uspto-grants-2016_06 |
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