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| | 1,3-Dihydro-1-methyl-4-(2-quinolyl)-2H-imidazol-2-one Basic information |
| | 1,3-Dihydro-1-methyl-4-(2-quinolyl)-2H-imidazol-2-one Chemical Properties |
| Melting point | 268-270°C (dec.). |
| | 1,3-Dihydro-1-methyl-4-(2-quinolyl)-2H-imidazol-2-one Usage And Synthesis |
| Description | A second alkaloid present in Macrorungia longistrobus C. B. Cl., this base forms
light yellow prisms when recrystallized from MeOH. It yields coloured salts and
derivatives, e.g. the hydrochloride as orange-red needles, decomposing above
290°C; the perchlorate as light yellow plates from MeOH, also decomposing
above 290°C; methiodide, orange prisms from MeOH, decomposing above 290°C
and the picrate, yellow needles, decomposing above 250°C. The ultraviolet
spectra of the alkaloid have been extensively studied. In neutral solution (EtOH),
the absorption maxima are at 220, 284, 301 and 354 mt.!; in acid solution (0.2
N/HCl-EtOH), they occur at 203, 225, 253, 300 and 413 mt.! while in alkaline
solution (0.1 N/NaOH-EtOH) they are at 227,283,323 and 382 mt.!. The struc_x0002_ture, as determined from the mass spectrum, is l'-methyl-2:4'-(1'Himidazolyl)quinolin-2' -one. | | References | Arndt, Jordaan, Joynt.,!. Chem. Soc., 5969 (1964)
Joynt et ai., J. Chem. Soc., B, 980 (1966) |
| | 1,3-Dihydro-1-methyl-4-(2-quinolyl)-2H-imidazol-2-one Preparation Products And Raw materials |
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