A Convenient Synthesis of New Pyrazolo[4,3-d]pyrimidines and Their Fused Heterocycles

被引:12
作者
Rote, Ramhari V. [1 ]
Shelar, Deepak P. [1 ]
Patil, Sandeep R. [1 ]
Jachak, Madhukar N. [1 ]
机构
[1] Univ Pune, KTHM Coll, Organ Chem Res Ctr, Dept Chem, Nasik 422002, Maharashtra, India
关键词
POTENTIAL PURINE ANTAGONISTS; ADENOSINE RECEPTOR ANTAGONISTS; PYRAZOLO-TRIAZOLO-PYRIMIDINE; CROSS-COUPLING REACTION; PYRAZOLO<3,4-D>PYRIMIDINES; 1-ALKENYLBORANES; DERIVATIVES;
D O I
10.1002/jhet.2006
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of some fused heterocycles originated from pyrazolopyrimidines were synthesized using 4-amino1-methyl-3-propyl-1H-pyrazole-5-carboxamide as a starting material. The nucleophilic substitution reactions with different amino acids followed by cyclization and Suzuki-Miyaura cross-coupling reactions with different aryl boronic acids of 7-chloro-5-(4-chlorophenyl)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidine were performed. Also, the oxidative cyclization reactions of 1-(5-(4-chlorophenyl)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)hydrazine with different aldehydes in the presence of diacetoxy iodobenzene are described. All the synthesized compounds were characterized by analytical and spectroscopic methods.
引用
收藏
页码:815 / 823
页数:9
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