Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | 6,7-Diamino-4-(5-methoxy-2-methylanilino)-3-quinolinecarbonitrile | HCID 21956395 | — |
| Reactant | N-[7-amino-3-cyano-4-(5-methoxy-2-methylanilino)-6-quinolinyl]-N-[2-(4-morpholinyl)-ethyl]thiourea | HCID 21956423 | — |
| Reactant | N-[6-amino-3-cyano-4-(5-methoxy-2-methylanilino)-7-quinolinyl]-N'-[2-(4-morpholinyl)ethyl]thiourea | HCID 21956495 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178490287 | HCID 178490287 | — |
Reaction Steps
A mixture of 0.1 g (0.3 mmol) of 6,7-diamino-4-(5-methoxy-2-methylanilino)-3-quinolinecarbonitrile and 0.11 g (0.62 mmol) of 2-(4-morpholino)ethylisothiocyanate in 0.3 mL of dioxane is heated at 100° C. for 2 hours under nitrogen. The mixture is cooled and solvent is evaporated to dryness to yield an oil consisting of N-[7-amino-3-cyano-4-(5-methoxy-2-methylanilino)-6-quinolinyl]-N-[2-(4-morpholinyl)-ethyl]thiourea and N-[6-amino-3-cyano-4-(5-methoxy-2-methylanilino)-7-quinolinyl]-N′-[2-(4-morpholinyl)ethyl]thiourea. The oil is dissolved in 3.0 mL of ethanol. To this is added 0.3 g of mercuric oxide and 20 mg of sulphur powder and the resulting mixture is heated at reflux temperature for 2 hours. The product mixture is filtered hot through diatomaceous earth, washed with methanol and solvent is evaporated to yield an oil. The oil is purified by silica gel chromatography, utilizing a gradient of methylene chloride/methanol (95:5 to 85:15) to yield 0.062 g of 8-(5-methoxy-2-methylanilino)-2-{[2-(4-morpholinyl)ethyl]amino}imidazo[4,5-g]quinoline-7-carbonitrile as a pink solid, mp 148–150° C. (shrinks at 140° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105531B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-a42f072aa15d4da7a8e0d7211309171f |
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| Source note | uspto-grants-2006_09 |
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