一种新型的基于一锅异氰酸酯的四组分反应:高度官能化的1 H-吡唑并[ 1,2- b ]邻苯二甲酰基1,2-二羧酸酯和1 H-吡唑并[1,2 - a ]哒嗪-1的合成,2-二羧酸盐
摘要:
为有效合成结构上不同的1 H-吡唑并[ 1,2- b ]邻苯二甲酰基-1,2-二羧酸酯和1 H-吡唑并[ 1,2- a ]哒嗪-1,2-二羧酸酯已开发出新的方案通过水合肼,乙炔二羧酸二烷基酯,异氰酸酯和各种环酐(如琥珀酸酐,马来酸酐和邻苯二甲酸酐)在室温下于乙醇/丙酮(1:1)中以良好至中等的收率进行四组分反应。
One-pot three-component reaction of isocyanides, dialkyl acetylenedicarboxylates and phthalhydrazide: synthesis of highly functionalized 1H-pyrazolo[1,2-b]phthalazine-5,10-diones
作者:Mohammad Bagher Teimouri
DOI:10.1016/j.tet.2006.09.006
日期:2006.11
Protonation of the highly reactive 1:1 intermediate produced in the reactionbetween alkyl isocyanides and electron-deficient acetylenic esters with phthalhydrazide, leads to a vinylisonitrilium cation, which undergoes an addition reaction with the conjugate base of the phthalhydrazide to produce dialkyl 3-(alkylamino)-5,10-dioxo-5,10-dihydro-1H-pyrazolo[1,2-b]phthalazine-1,2-dicarboxylates in fairly
在烷基异氰化物和电子不足的炔属酸酯与邻苯二甲酰肼之间的反应中产生的高反应性1:1中间体的质子化导致乙烯基异腈鎓阳离子,该阳离子与邻苯二甲酰肼的共轭碱进行加成反应以生成3-(烷基氨基二烷基) )-5,10-二氧杂-5,10-二氢-1 H-吡唑并[ 1,2- b ]邻苯二甲酰基-1,2-二羧酸酯在室温下的产率很高。
A novel one-pot isocyanide-based four-component reaction: synthesis of highly functionalized 1H-pyrazolo[1,2-b]phthalazine-1,2-dicarboxylates and 1H-pyrazolo[1,2-a]pyridazine-1,2-dicarboxylates
作者:Sajjad Keshipour、Salman Shojaei、Ahmad Shaabani
DOI:10.1016/j.tet.2012.05.078
日期:2012.8
A new protocol has been developed for the efficient synthesis of structurally diverse 1H-pyrazolo[1,2-b]phthalazine-1,2-dicarboxylates and 1H-pyrazolo[1,2-a]pyridazine-1,2-dicarboxylates via a four-component reaction of hydrazine hydrate, dialkyl acetylenedicarboxylates, isocyanides and various cyclic anhydrides such as succinic anhydride, maleic anhydride and phthalicanhydride in ethanol/acetone
为有效合成结构上不同的1 H-吡唑并[ 1,2- b ]邻苯二甲酰基-1,2-二羧酸酯和1 H-吡唑并[ 1,2- a ]哒嗪-1,2-二羧酸酯已开发出新的方案通过水合肼,乙炔二羧酸二烷基酯,异氰酸酯和各种环酐(如琥珀酸酐,马来酸酐和邻苯二甲酸酐)在室温下于乙醇/丙酮(1:1)中以良好至中等的收率进行四组分反应。