3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile

Base Information

Chemical Name:3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile
CAS No.:1345014-46-1
Molecular Formula:C₂₁H₁₆N₄O
Molecular Weight:340.384
Hs Code.:

Synonyms:3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile

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Chemical Property of 3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile

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Technology Process of 3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile

There total 7 articles about 3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile 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: 26.0%

: 1345014-05-2
tert-butyl 4-(methylsulfonyl)-5-oxo-2-phenyl-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate

: 2237-30-1
m-cyanoaniline

: 1345014-46-1
3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile

Guidance literature:: tert-butyl 4-(methylsulfonyl)-5-oxo-2-phenyl-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate; m-cyanoaniline; In ethanol; at 70 ℃; for 96h;

With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 4h;

Reference yield:

: C₂₆H₂₄N₄O₃

: 1345014-46-1
3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile

Guidance literature:: With trifluoroacetic acid; In chloroform; at 20 ℃; for 1h;
DOI:10.1016/j.tetlet.2013.06.016

Reference yield:

: 1345013-95-7
tert-butyl 4-(methylthio)-5-oxo-2-phenyl-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate

: 1345014-46-1
3-[(5-oxo-2-phenyl-5,6,7,8-tetrahydro-1,6-naphthyridin-4-yl)amino]benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2.5 h / 5 - 20 °C

2.1: ethanol / 96 h / 70 °C

2.2: 4 h / 20 °C

With 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane;