5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile

Base Information

• Chemical Name: 5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile
• CAS No.: 1357459-19-8
• Molecular Formula: C₃₀H₁₉N₅O₂
• Molecular Weight: 481.513

Synonyms:5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile

Chemical Property of 5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile

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Technology Process of 5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile

There total 4 articles about 5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 70.0%

1,2-dihydro-2-imino-6-(2-imino-2H-chromen-3-yl)-1,4-diphenylpyridine-3-carbonitrile (1357459-17-6) + ethyl 2-cyanoacetate (105-56-6) → 5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile (1357459-19-8)

Guidance literature:

With piperidine; In ethanol; for 6h; Reflux;

DOI:10.1002/jhet.716

Reference yield:

3-(2-imino-2H-chromen-3-yl)-1-phenyl-3-(phenylamino)prop-2-en-1-one (1357459-14-3) → 5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile (1357459-19-8)

Guidance literature:

Multi-step reaction with 2 steps

1: piperidine / ethanol / 6 h / Reflux

2: piperidine / ethanol / 6 h / Reflux

With piperidine; In ethanol;

DOI:10.1002/jhet.716

Reference yield:

acetophenone (98-86-2) → 5-amino-1,7-dihydro-2-(2-imino-2H-chromen-3-yl)-7-oxo-1,4-diphenyl-1,8-naphthyridine-6-carbonitrile (1357459-19-8)

Guidance literature:

Multi-step reaction with 3 steps

1: piperidine / N,N-dimethyl-formamide / 8 h / Reflux

2: piperidine / ethanol / 6 h / Reflux

3: piperidine / ethanol / 6 h / Reflux

With piperidine; In ethanol; N,N-dimethyl-formamide;

DOI:10.1002/jhet.716

upstream raw materials:

3-(2-imino-2H-chromen-3-yl)-1-phenyl-3-(phenylamino)prop-2-en-1-one

1,2-dihydro-2-imino-6-(2-imino-2H-chromen-3-yl)-1,4-diphenylpyridine-3-carbonitrile

ethyl 2-cyanoacetate

acetophenone

Downstream raw materials:

5,6,7,8-tetrahydro-2-(2-imino-2H-chromen-3-yl)-1,4-diphenyl-6,8-dithioxopyrimido[5,4-c][1,8]naphthyridin-9(1H)-one

2-(2-imino-2H-chromen-3-yl)-1,4-diphenylpyrimido[5,4-c][1,8]naphthyridine-8,9(1H,7H)-dione

6,8-diamino-7-(1H-benzo[d]imidazol-2-yl)-2-(2-imino-2H-chromen-3-yl)-1,4-diphenylpyrido[2,3-c][1,6]naphthyridin-9(1H)-one

6-benzyl-2-(2-imino-2H-chromen-3-yl)-1,4-diphenylpyrimido[5,4-c][1,8]naphthyridine-8,9(1H,5H)-dione

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