863786-32-7

Upstream product

• 104-12-1 p-chlorphenylisocyanate 
• 90543-08-1 1-Phenyl-5-(triphenylphosphoranylidenamino)-1,2,3-triazol-4-carbonsaeure-ethylester 
• 20271-37-8 ethyl 5-amino-1-phenyl-1,2,3-triazole-4-carboxylate 

Downstream Products

• 863786-38-3 5-[N'-(4-chloro-phenyl)-N''-isopropyl-guanidino]-1-phenyl-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester 
• 1356190-32-3 6-(4-chlorophenyl)-3,6-dihydro-5-[(p-fluorophenyl)sulfinyl]-3-phenyl-1,2,3-triazolo[4,5-d]pyrimidine-7-one 
• 1356190-38-9 6-(4-chlorophenyl)-3,6-dihydro-5-[(p-fluorophenyl)sulfonyl]-3-phenyl-1,2,3-triazolo[4,5-d]pyrimidine-7-one 
• 1356190-26-5 6-(4-chlorophenyl)-3,6-dihydro-5-[(p-fluorophenyl)thio]-3-phenyl-1,2,3-triazolo-[4,5-d]pyrimidine-7-one 
• 1364422-37-6 6-(4-chlorophenyl)-5-[(2-chlorophenyl)thio]-3,6-dihydro-3-phenyl-1,2,3-triazolo[4,5-d]pyrimidine-7-one 
• 1364422-31-0 6-(4-chlorophenyl)-3,6-dihydro-3-phenyl-5-phenylthio-1,2,3-triazolo[4,5-d]pyrimidine-7-one 
• 1364422-40-1 6-(4-chlorophenyl)-3,6-dihydro-5-[(4-methylphenyl)thio]-3-phenyl-1,2,3-triazolo[4,5-d]pyrimidine-7-one 
• 1364422-34-3 6-(4-chlorophenyl)-5-[(4-chlorophenyl)thio]-3,6-dihydro-3-phenyl-1,2,3-triazolo[4,5-d]pyrimidine-7-one 
• 875485-67-9 5-(4-chlorophenyl)amino-3,6-dihydro-3-phenyl-6-(triphenylphosphoranylidene)amino-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one 
• 875485-64-6 6-amino-5-(4-chlorophenyl)amino-3,6-dihydro-3-phenyl-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-one 

Relevant academic research and scientific papers

Iminophosphorane-mediated efficient synthesis of new fluorine-containing triazolo[4,5-d]pyrimidin-7-ones

The carbodiimides 3, obtained from aza-Wittig reactions of the corresponding iminophosphorane 2 with 1 equiv. of aromatic isocyanates, were allowed to react in the presence of a catalytic amount of potassium carbonate or EtO-Na+ with

New efficient synthesis of 5,6-disubstituted-3-phenyl-1,2,3-triazolo[4,5-d] pyrimidin-7-ones via a tandem aza-Wittig reaction

Twelve novel 5,6-disubstituted-3-phenyl-1,2,3-triazolo[4,5-d]pyrimidine-7- ones 5a-5l were designed and successfully synthesized via tandem aza-Wittig and annulation reactions of the corresponding iminophosphorances 2, aromatic isocyanate, and substituted

Iminophosphorane-mediated efficient synthesis of new tricyclic 3,5-dihydro-1,2,3-triazolo[4,5-d]-1,2,4-triazolo[1,5-a]pyrimidin-9-ones

The carbodiimides 2, obtained from aza-Wittig reactions of iminophosphorane 1 with aromatic isocyanates, reacted with hydrazine to give selectively 6-amino-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-ones 5. Compounds 5 were further transformed to iminophosphoran

A selective synthesis of 3,6-dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7- ones

The carbodiimides 2, obtained from aza-Wittig reactions of iminophosphorane 1 with aromatic isocyanates, reacted with primary amine RNH2 (R ≠ H, Me) to produce isolable guanidine intermediates 3, which were further treated with sodium ethoxide

Base-catalyzed, efficient synthesis of 5-substituted 3,6-dihydro-7H-1,2,3- triazolo[4,5-d]pyrimidin-7-ones

The carbodiimides 2, obtained from aza-Wittig reactions of iminophosphorane 1 with aromatic isocyanates, reacted with secondary amines or ROH to give 5-dialkylamino or 5-alkoxy 7H-1,2,3-triazolo[4,5-d]pyrimidin-7-ones 4 in the presence of a catalytic amou