Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 86633712 | HCID 86633712 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178517323 | HCID 178517323 | 75.5% |
Reaction Steps
1,1′-Carbonyldiimidazole (3.20 g, 19.7 mmol) was added to 2-chloro-N4-(pyridin-3-ylmethyl)quinoline-3,4-diamine (5.09 g, 17.9 mmol) in THF (100 mL), and the resulting suspension was heated at 80° C. for three days. An analysis by LC/MS indicated the presence of starting material, and pyridine (100 mL) and additional 1,1′-carbonyldiimidazole (1 equivalent) were added. The reaction was stirred for two hours at 80° C., and additional 1,1′-carbonyldiimidazole (1 equivalent) was added. The reaction was stirred overnight at 80° C. and allowed to cool; a solid was present. Diethyl ether (50 mL) was added, and the solid was isolated by filtration and dried under vacuum to provide 4.2 g of 4-chloro-1-(pyridin-3-ylmethyl)-1H-imidazo[4,5-c]quinolin-2-ol as a gray solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088790B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-22f22abd7e9542c1a0ad99a0d57f9a43 |
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| Source note | uspto-grants-2012_01 |
|---|