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[双官能团四氢异喹啉的合成与环合反应]

[Syntheses and ring-closures of difunctional tetrahydroisoquinolines].

作者信息

Zalán Zita

机构信息

Szegedi Tudományegyetem, Gyógyszerkémiai Intézet, Szeged.

出版信息

Acta Pharm Hung. 2006;76(3):155-64.

Abstract

Starting from homoveratrylamine and N-protected amino acids 1,2,3,4-tetrahydroisoquinoline diamines were prepared by a convenient four-step process. This synthetic method was successfully extended to substituted beta-alanine and homoveratrylamine derivatives. In the case of the 1'-methyl-substituted derivatives, the reducing agent applied and the sequence of the reduction and deprotection steps proved to have marked effects on the formation of the possible diamine diastereomers. By N-amination of the corresponding amino alcohols, tetrahydroisoquinoline hydrazino alcohol regioisomers were prepared. Condensation products of the prepared tetrahydroisoquinoline 1,2- and 1,3-diamines containing a primary amino group with aromatic aldehydes proved to participate in three-component ring-chain tautomeric equilibria. The tautomeric equilibrium was sensitive to the electronic effects of the aromatic substituents, the ring size and the methyl substituents of the skeleton. By N-substitution reactions of 1-(Cbz-aminomethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline with isocyanates and isothiocyanates, the corresponding urea or thiourea derivatives were obtained some derivatives of which showed a remarkable MDR modulating activity. By ring-closures of tetrahydroisoquinoline diamines and hydrazino alcohols with phosphorus-containing reagents, saturated 1,3,2-diazaphosphino[6,1-a]isoquinolines, and 1,3,4,2-oxadiazaphosphino[5,4-a]- and [4,5-b]isoquinolines as the first representatives of these ring systems were prepared. The conformational behaviour of these compounds was studied by NMR and X-ray diffractional analyses.

摘要

从高藜芦胺和N-保护的氨基酸出发,通过简便的四步过程制备了1,2,3,4-四氢异喹啉二胺。这种合成方法成功地扩展到了取代的β-丙氨酸和高藜芦胺衍生物。对于1'-甲基取代的衍生物,所使用的还原剂以及还原和脱保护步骤的顺序对可能的二胺非对映异构体的形成有显著影响。通过相应氨基醇的N-胺化反应,制备了四氢异喹啉肼醇区域异构体。所制备的含有伯氨基的四氢异喹啉1,2-二胺和1,3-二胺与芳香醛的缩合产物被证明参与了三组分环链互变异构平衡。该互变异构平衡对芳香取代基的电子效应、骨架的环大小和甲基取代基敏感。通过1-(Cbz-氨基甲基)-6,7-二甲氧基-1,2,3,4-四氢异喹啉与异氰酸酯和异硫氰酸酯的N-取代反应,获得了相应的脲或硫脲衍生物,其中一些衍生物表现出显著的多药耐药性调节活性。通过用含磷试剂使四氢异喹啉二胺和肼醇环化,制备了饱和的1,3,2-二氮杂膦基[6,1-a]异喹啉以及1,3,4,2-氧杂二氮杂膦基[5,4-a]-和[4,5-b]异喹啉,作为这些环系的首批代表物。通过核磁共振和X射线衍射分析研究了这些化合物的构象行为。

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