Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Aminoisoquinoline | HCID 70766 | — |
| Reactant | 1-Ethoxyethanol | HCID 10129898 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | 4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrile | HCID 10586676 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 9924834 | HCID 9924834 | 28% |
Reaction Steps
A mixture of 0.249 g of 4-chloro-6,7-dimethoxy-quinolin-3-carbonitrile, 0.288 g of 5-aminoisoquinoline, 0.020 g of pyridine hydrochloride, and 10 ml of ethoxyethanol was heated under nitrogen in a sealed tube at 200° C. for 2 hours. The mixture was cooled and added to 100 ml of water. To this mixture was added sodium carbonate to pH 9. The product was collected, washed with water, and dried to give 0.100 g of 4-(isoquinolin-5-ylamino)-6,7-dimethoxy-quinoline-3-carbonitrile as a solid, mp 140° C. (decomposed); mass spectrum (EI, m/e): M 356.1279.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06288082B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-337a24f86d45414cab90c8d406e52453 |
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| Source note | uspto-grants-2001_09 |
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