Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 1-((3-Aminoquinolin-4-yl)amino)-2-methylpropan-2-ol | HCID 14986941 | — |
| Edukt | 1,3-dimethoxycarbonyl-O-methylisourea | HCID 85348789 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 86626308 | HCID 86626308 | — |
Reaktionsschritte
A mixture of 1-[(3-amino-4-quinolinyl)amino]-2-methyl-2-propanol (1.0 g, 4.3 mmol), 1,3-dimethoxycarbonyl-O-methylisourea (prepared according to the general method of Viswanathan, N. Indian Patent No. 168,784, 1.64 g, 8.64 mmol), acetic acid (1.3 g, 22 mmol), and p-toluenesulfonic acid (0.82 g, 4.3 mmol) in methanol (20 mL) was heated at reflux for 16 hours. The volatiles were removed under reduced pressure, and the residue was dissolved in chloroform (100 mL). The solution was washed sequentially with water (100 mL), aqueous sodium carbonate (100 mL of 4% w/w), water (100 mL), and brine (100 mL) and then concentrated under reduced pressure. The residue was purified by automated flash chromatography (40+M silica cartridge, eluting with 0% to 25% CMA in chloroform) followed by recrystallization from acetonitrile to provide 0.64 g of methyl [1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]carbamate as a white solid, mp 225° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08143270B2 |
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| Quelldatensatz | uspto-grants-2012_03 |
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| ORD ID | ord-472c74c0e8fe4f3da8c4ec9e479e1b28 |
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| Quellennotiz | uspto-grants-2012_03 |
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