(S)-1-(6,8-ジメトキシ-1,3-ジオキソロ[4,5-h]キノリン-7-イル)-3-メチル-2,3-ブタンジオール 化学特性,用途語,生産方法
説明
A further alkaloid from the roots of Orixa japonica Thunb., this quinoline base
is obtained as colourless needles from EtOH. It is soluble in Et20, CHC13, EtOH
and AcOEt but insoluble in petroleum ether. It has a specific rotation of [α]
17
D +
83.29° (CHC13). The aurichloride has been prepared as pale yellow needles, m.p.
lS5°C (dec.). Two methoxyl groups, a methylenedioxy group and a secondary
and tertiary hydroxyl group are present.
参考文献
Terasaka., J. Pharrn. Soc., Japan, 51, 99 (1931)
Terasaka., ibid, 53, 219 (1933)
Terasaka., Chern. Pharrn. Bull., 8, 523 (1960)
(S)-1-(6,8-ジメトキシ-1,3-ジオキソロ[4,5-h]キノリン-7-イル)-3-メチル-2,3-ブタンジオール 上流と下流の製品情報
原材料
準備製品