1069094-28-5

Upstream product

• 1188-33-6 N,N-dimethylformamide diethyl diacetal 

Downstream Products

• 1201629-31-3 11-(benzyl)-1,6-dihydro-4-oxo-4H-pyrimido[5',4':5,6]pyrido[3,2-b]indolium-11 chloride 
• 1201629-40-4 11-benzyl-6-methyl-4-oxo-4,6-dihydro-3H-pyrimido-[5',4':5,6]pyrido[3,2-b]indol-11-ium chloride 
• 1201629-39-1 11-benzyl-6-methyl-6,11-dihydro-4H-pyrimido[5',4':5,6]pyrido[3,2-b]indol-4-one 
• 1201629-34-6 11-benzyl-3-methyl-4,11-dihydro-3H-pyrimido[5',4':5,6]pyrido[3,2-b]indol-4-one 
• 1201629-36-8 11-benzyl-3,6-bis(2-methoxy-2-oxoethyl)-4-oxo-4,6-dihydro3H-pyrimido-[5',4':5,6]pyrido[3,2-b]indol-11-ium iodide 
• 1201629-38-0 11-benzyl-3,6-dimethyl-4-oxo-4,6-dihydro-3H-pyrimido-[5',4':5,6]pyrido[3,2-b]indol-11-ium methyl sulfate 
• 1201629-35-7 11-benzyl-3,6-dimethyl-4-oxo-4,6-dihydro-3H-pyrimido-[5',4':5,6]pyrido[3,2-b]indol-11-ium iodide 
• 1201629-32-4 11-benzyl-3-methyl-4-oxo-4,6-dihydro-3H-pyrimido-[5',4':5,6]pyrido[3,2-b]indol-11-ium iodide 

Relevant academic research and scientific papers

Synthesis of derivatives of the new heterocyclic system pyrimido[5',4':5,6]pyrido[3,2-b]indole

Derivatives of the new heterocyclic system 1,11-dihydro-4H-pyrimido[5',4': 5,6]pyrido[3,2-b]indol-4-one were synthesized by the reactions of 2-(2-cyanoprop-2-enylidene)indolin-3-ones, bearing the primary and secondary amino groups in position 3 of the side chain, with DMF diethyl acetal. A scheme of formation of the synthesized compounds was proposed and confirmed.