243666-01-5

Upstream product

• 371-40-4 4-fluoroaniline 
• 75562-68-4 2-bromo-1-(p-methoxyphenyl)ethylidenemalononitrile 
• 243665-83-0 2-amino-1-(4-fluoro-phenyl)-4-(4-methoxy-phenyl)-1H-pyrrole-3-carbonitrile 
• 243665-95-4 7-(4-fluoro-phenyl)-5-(4-methoxy-phenyl)-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one 

Downstream Products

• 243666-07-1 [7-(4-fluoro-phenyl)-5-(4-methoxy-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-hydrazine 
• 507273-52-1 7-(4-fluorophenyl)-9-(4-methoxyphenyl)tetrazolo[1,5-c]-7H-pyrrolo[3,2-e]pyrimidine 
• 1006628-70-1 7-(4-fluorophenyl)-9-(4-methoxyphenyl)-7H-pyrrolo[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine 

Relevant academic research and scientific papers

Syntheses of 1,3-disubstituted-5a-hydropyrrolo[2,3-d]quinazolino[3,2-e] pyrimidin-6(5H)-ones: A comparison of conventional and microwave technique

An exclusive new ring system of 1,3-disubstituted-5a-hydropyrrolo[2,3-d] quinazolino [3,2-e]pyrimidin-6(5H)-ones 4 has been synthesised from 4-chloropyrrolo[2,3-d]pyrimidines 2 which are prepared using phase transfer catalysts. The synthesis 4 highlights

Synthesis and reactions of fluoroaryl substituted 2-amino-3- cyanopyrroles and pyrrolo[2,3-d]pyrimidines

Some fluoroaryl substituted 2-amino-3-cyanopyrroles 2 were synthesized from the reaction between (2-bromo-1-arylalkylidene)propanedinitriles 1 and fluoroaryl substituted aromatic amines under Gewald reaction condition, which on reaction with formamide and