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| | 2β-(1-Hydroxy-1-methylethyl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinoline Basic information |
| | 2β-(1-Hydroxy-1-methylethyl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinoline Chemical Properties |
| | 2β-(1-Hydroxy-1-methylethyl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinoline Usage And Synthesis |
| Description | This furoquinoline alkaloid was first isolated from Platydesma campanulata
Mann and subsequently found in Geijera salicifolia Schott. It crystallizes from
C6H6-light petroleum in white needles and has [α]25D + 43° (CHCl3). The ultraviolet spectrum in EtOH contains several absorption maxima at 229.3, 238.1,
253.5,262.3,272,283,307.2 and 320.5 mJ.l. with a shoulder at 294.5 mil. The
methiodide forms colourless plates from EtOH, m.p. 1 62-4°C and the picrate
has m.p. 107-9°C after softening at 93°C. The optically inactive base, obtained
as prisms from a mixture of MeOH and isopropyl ether, melts at 137 -SoC and
gives a picrate melting over a very wide temperature range from 96-l22°C. | | Definition | ChEBI: Platydesmine is an organonitrogen heterocyclic compound, an oxacycle and an organic heterotricyclic compound. | | References | Werner, Schuer., Tetrahedron, 19, 1293 (1963)
Bowman, Grundon., Chem. Commun., 334 (1965)
Bowman, Grundon.,J. Chem. Soc., C, 1504 (1966)
Johns, Lamberton., Austral. J. Chem., 19,1991 (1966)
Boyd, Grunson., Tetrahedron Lett., 2637 (1967) |
| | 2β-(1-Hydroxy-1-methylethyl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinoline Preparation Products And Raw materials |
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