1983
DOI: 10.1002/jhet.5570200612
|View full text |Cite
|
Sign up to set email alerts
|

Displacement reactions of 5‐chloro‐4‐phenylazopyrazoles

Abstract: 3‐Methyl or 3‐phenyl‐5‐chloro‐1‐phenyl‐4‐phenylazopyrazole with primary amines, sodium polysulfide and sodium azide yielded amines, disulfides and 2,4‐dihydropyrazolo[3,4‐d]‐1,2,3‐triazoles respectively. 4‐Amino‐5‐anilino‐1,3‐diphenylpyrazole was also prepared and characterized.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1984
1984
2011
2011

Publication Types

Select...
3
2

Relationship

0
5

Authors

Journals

citations
Cited by 7 publications
(1 citation statement)
references
References 7 publications
0
1
0
Order By: Relevance
“…8 The 4,5-diaminopyrazoles were reported by preparation of different methods. [9][10][11] In order to find more new N and S containing pyrazole heterocycles with biological activity, here we synthesize a series of new compounds by cyclization of 4,5-diamino pyrazole with different reactions.…”
Section: Introductionmentioning
confidence: 99%
“…8 The 4,5-diaminopyrazoles were reported by preparation of different methods. [9][10][11] In order to find more new N and S containing pyrazole heterocycles with biological activity, here we synthesize a series of new compounds by cyclization of 4,5-diamino pyrazole with different reactions.…”
Section: Introductionmentioning
confidence: 99%