Document Details

Document Type : Article In Journal 
Document Title :
Synthesis and biological evaluation of some new triazolo- and triazinophthalazines
Synthesis and biological evaluation of some new triazolo- and triazinophthalazines
 
Document Language : Arabic 
Abstract : Abstract: Condensation of hydralazine 1 with ethyl oxalate afforded triazinodione 3 or s-triazolo derivative 4, while with alpha-bromo ketones, 1,2-cyclohexanedione and pyridine keto acid it gave the as-triazino derivatives a-a respectively. Reaction of 1 with bromo esters yield the corresponding 3-bromo-alkyl s-triazolophthalazines 9. Condensation of 9a with hydrazine hydrate followed by acetylacetone afforded the pyrazole derivative ii. Cyclization of 1 with acid chlorides or ketones gave the appropriate 3-substitutes s-triazolophthalazines. With chloromalonic acid ester, 1 yielded the triazino-triazolo derivative 18, while with pyridine acetal it gave the his s-triazolophthalazine 19. 
Journal Name : Source: AFINIDAD 
Volume : 55 
Issue Number : 475 
Publishing Year : 1998 AH  
Added Date : Saturday, June 14, 2008 

Researchers

Researcher Name (Arabic)Researcher Name (English)Researcher TypeDr GradeEmail
سالم أحمد باسيف Researcher  

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