1415648-01-9

Upstream product

• 13580-88-6 4-aminophthalazin-1(2H)-one 
• 637-87-6 1-Chloro-4-iodobenzene 
• 17763-70-1 methyl 2-(trifluoromethylsulfonyloxy)benzoate 
• 610-97-9 o-iodo-methyl-benzoic acid 
• 610-96-8 methyl chlorobenzoate 
• 1346229-07-9 4-(tert-butylamino)phthalazin-1(2H)-one 
• 610-94-6 2-bromobenzoic acid methyl ester 
• 86671-87-6 2-(4-Chlorophenyl)-1(2H)-phthalazinone-4-carboxylic acid chloride 
• 1415647-89-0 3-(4-chlorophenyl)-4-oxo-3,4-dihydrophthalazine-1-carbonyl azide 
• 86662-15-9 3-(4-chlorophenyl)-4-oxo-3,4-dihydrophthalazine-1-carboxylic acid 
• 97458-95-2 methyl 4-oxo-3-(4-chlorophenyl)-3,4-dihydrophthalazine-1-carboxylate 
• 791638-32-9 2-[Methoxy(oxo)acetyl]benzoesaeure 
• 14736-50-6 o-(methoxycarbonylmethyl)benzoic acid 

Relevant academic research and scientific papers

Multicomponent synthesis of 4-aminophthalazin-1(2 H)-ones by palladium-catalyzed isocyanide insertion

4-Aminophthalazin-1(2H)-ones (APOs) are underexplored heterocyclic compounds with promising and diverse biological activities. The classical synthesis of these compounds is tedious and does not allow the regioselective introduction of substituents. Here,

Facile synthesis of novel 7-aminofuro- and 7-aminothieno[2,3-d]pyridazin- 4(5H)-one and 4-aminophthalazin-1(2H)-ones

We hereby report the synthesis of a novel class of compounds, 7-aminofuro- and 7-aminothieno[2,3-d]pyridazin-4(5H)-one and 4-aminophthalazin-1(2H)-ones starting from methyl 2-(2-methoxy-2-oxoethyl)furan- and thiophene-3-carboxylate and methyl 2-(2-methoxy