The Reaction of Ethyl 2-oxo-2H-chromene-3-carboxylate with Hydrazine Hydrate

被引:15
作者
Abdel-Aziz, Hatem A. [1 ,2 ]
Elsaman, Tilal [1 ]
Attia, Mohamed I. [1 ,3 ]
Alanazi, Amer M. [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh 11451, Saudi Arabia
[2] Natl Res Ctr, Dept Appl Organ Chem, Cairo 12622, Egypt
[3] Natl Res Ctr, Dept Med & Pharmaceut Chem, Cairo 12622, Egypt
关键词
salicylaldehyde azine; malonohydrazide; coumarins; hydrazides/hydrazones; ring-opening; ANTIMICROBIAL EVALUATION; BIOLOGICAL EVALUATION; CONVENIENT SYNTHESIS; DERIVATIVES; 1,2,4-TRIAZOLE; PYRAZOLE; 1,3,4-OXA(THIA)DIAZOLE;
D O I
10.3390/molecules18022084
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although salicylaldehyde azine (3) was reported in 1985 as the single product of the reaction of ethyl 2-oxo-2H-chromene-3-carboxylate (1) with hydrazine hydrate, we identified another main reaction product, besides 3, which was identified as malono-hydrazide (4). In the last two decades, however, some articles have claimed that this reaction afforded exclusively hydrazide 2 and they have reported the use of this hydrazide 2 as a precursor in the syntheses of several heterocyclic compounds and hydrazones 6. We reported herein a study of the formation of 2 and a facile route for the synthesis of the target compounds N'-arylidene-2-oxo-2H-chromene-3-carbohydrazides 6a-f.
引用
收藏
页码:2084 / 2095
页数:12
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