Chemistry of antipyrine

被引:37
作者
Elattar, Khaled M. [1 ]
Fadda, Ahmed A. [1 ]
机构
[1] Mansoura Univ, Dept Chem, Fac Sci, El Gomhoria St, Mansoura 35516, Egypt
关键词
Antipyrine; reactions; synthesis; synthetic and biological importance; HETEROCYCLIC SYNTHESIS SYNTHESIS; PHOTOCHEMICAL DECOMPOSITION; PHENAZONE DERIVATIVES; AROMATIC-ALDEHYDES; COLOR-REACTION; ACID; ENAMINONITRILES; CORROSION; PYRAZOLE; ACCESS;
D O I
10.1080/00397911.2016.1211703
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This review is a literature survey of antipyrine, considered as one of the most valuable compounds in the fields of organic and medicinal chemistry. The biological importance, synthetic procedures, and reactions are discussed. Generally, the preparation of antipyrine was reported through the methylation of the corresponding 1H-pyrazolone following different reaction conditions. The reactions, in general, are electrophilic substitutions at C-4-position of pyrazolone. The mechanistic pathways of the reactions are surveyed. [GRAPHICS] .
引用
收藏
页码:1567 / 1594
页数:28
相关论文
共 139 条
[1]  
Abreu M.E., 1991, US Patent, Patent No. [5063245A, 5063245]
[2]  
AFSAH EM, 1995, PHARMAZIE, V50, P567
[3]   ON THE REACTION OF PHENAZONE AND LITHIATED PHENAZONE WITH ARYL-CARBONYL DERIVATIVES [J].
AKGUN, E ;
PINDUR, U .
MONATSHEFTE FUR CHEMIE, 1984, 115 (02) :197-203
[4]   SYNTHESIS AND STRUCTURE OF PYRAZOLYL CATIONS WITH POLYMETHINE AND METHANE FRAMEWORK [J].
AKGUN, E ;
KAMPCHEN, T ;
PINDUR, U .
MONATSHEFTE FUR CHEMIE, 1983, 114 (02) :219-225
[5]   THE STRUCTURE AND THE CONFORMATION OF ARYL-SUBSTITUTED (PYRAZOLINONYL)(HYDROXYPYRAZOLYLIUM)METHANE PERCHLORATES [J].
AKGUN, E ;
PINDUR, U .
ARCHIV DER PHARMAZIE, 1984, 317 (09) :737-742
[6]   Studies on 3-Oxoalkanenitriles: Novel Rearrangement Reactions Observed in Studies of the Chemistry of 3-Heteroaroyl-3-Oxoalkanenitriles as Novel Routes to 2-Dialkylaminopyridines [J].
Al-Matar, Hamad M. ;
Khalil, Khaled D. ;
Al-Kanderi, Mona F. ;
Elnagdi, Mohamed H. .
MOLECULES, 2012, 17 (01) :897-909
[7]  
[Anonymous], 1992, Pharm. Chem. J., DOI DOI 10.1007/BF00772907
[8]  
[Anonymous], 1989, KHIM GETEROTSIKLICH, V9, P1243
[9]  
[Anonymous], 2013, J CHEM-NY
[10]  
[Anonymous], 1982, ZH OBSHCH KHIM, V52, P1146