【药物名称】DuP-654
化学结构式(Chemical Structure):
参考文献No.5337
标题:2-Substituted-1-naphthols as 5-lipoxygenase inhibitors
作者:Batt, D.G. (E.I. Du Pont de Nemours & Co.)
来源:AU 8657186; EP 0201071; ES 8801780; US 4833164
合成路线图解说明:

Alkylation of the sodium salt of 1-naphthol with benzyl bromide provides DuP-654. Alternatively, condensation of 1-tetralone (I) with benzaldehyde (II) in the presence of potassium hydroxide yields 2-benzylidene-1-tetralone (III), which may be isomerized to DuP-654 using rhodium chloride or a soluble iridium complex. A mixture of (I) and (II) may also be directly converted to DuP-654 by treating with potassium tert-butoxide in refluxing tert-butanol.

参考文献No.109642
标题:DuP-654
作者:Harris, R.R.; Batt, D.G.; Galbraith, W.; Gans, K.R.; Jaffee, B.D.; Kerr, J.S.; Ackerman, N.R.; Mackin, W.M.
来源:Drugs Fut 1989,14(11),1040
合成路线图解说明:

Alkylation of the sodium salt of 1-naphthol with benzyl bromide provides DuP-654. Alternatively, condensation of 1-tetralone (I) with benzaldehyde (II) in the presence of potassium hydroxide yields 2-benzylidene-1-tetralone (III), which may be isomerized to DuP-654 using rhodium chloride or a soluble iridium complex. A mixture of (I) and (II) may also be directly converted to DuP-654 by treating with potassium tert-butoxide in refluxing tert-butanol.

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