4H-Imidazo(4,5-c)(1,8)naphthyridin-4-one, 1,5-dihydro-5-phenyl-1-(phenylmethyl)-

Base Information

Chemical Name:4H-Imidazo(4,5-c)(1,8)naphthyridin-4-one, 1,5-dihydro-5-phenyl-1-(phenylmethyl)-
CAS No.:139339-08-5
Molecular Formula:C₂₂H₁₆N₄O
Molecular Weight:352.395
Hs Code.:
DSSTox Substance ID:DTXSID30161017
Nikkaji Number:J454.446C
Wikidata:Q83029375
ChEMBL ID:CHEMBL330161
Mol file:139339-08-5.mol

Synonyms:1,5-Dihydro-5-phenyl-1-(phenylmethyl)-4H-imidazo(4,5-c)(1,8)naphthyridin-4-one;4H-Imidazo(4,5-c)(1,8)naphthyridin-4-one, 1,5-dihydro-5-phenyl-1-(phenylmethyl)-;139339-08-5;CHEMBL330161;SCHEMBL7280534;DTXSID30161017;LS-80029;1-Benzyl-1,5-dihydro-5-phenyl-1,3,5,6-tetraaza-4H-benz[e]inden-4-one

Suppliers and Price of 4H-Imidazo(4,5-c)(1,8)naphthyridin-4-one, 1,5-dihydro-5-phenyl-1-(phenylmethyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 4H-Imidazo(4,5-c)(1,8)naphthyridin-4-one, 1,5-dihydro-5-phenyl-1-(phenylmethyl)-

Chemical Property:

Vapor Pressure:3.88E-16mmHg at 25°C
Boiling Point:637.2°Cat760mmHg
Flash Point:339.2°C
Density:1.29g/cm³
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:352.13241115
Heavy Atom Count:27
Complexity:528

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CN2C=NC3=C2C4=C(N=CC=C4)N(C3=O)C5=CC=CC=C5

Technology Process of 4H-Imidazo(4,5-c)(1,8)naphthyridin-4-one, 1,5-dihydro-5-phenyl-1-(phenylmethyl)-

There total 6 articles about 4H-Imidazo(4,5-c)(1,8)naphthyridin-4-one, 1,5-dihydro-5-phenyl-1-(phenylmethyl)- 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: 15.0%

: 139339-08-5
1-Benzyl-5-phenyl-1H-imidazo[4,5-c][1,8]naphthyridin-4(5H)-one

Guidance literature:

Reference yield:

: 138305-19-8
1-phenyl-2H-pyrido<2,3-d><1,3>oxazine-2,4(1H)-dione

: 139339-08-5
1-Benzyl-5-phenyl-1H-imidazo[4,5-c][1,8]naphthyridin-4(5H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) 60percent NaH / 1.) DMA, 0 deg C, 2.) DMA, 100 deg C,30 min

2: 49 percent / POCl₃ / 1 h / Heating

3: 87 percent / H₂O; tetrahydrofuran / 0.5 h / Ambient temperature

4: sodium hydrosulfite / ethanol; H₂O / 0.17 h / 80 °C

5: 1 h / Heating

With sodium disulfite; sodium hydride; trichlorophosphate; In tetrahydrofuran; ethanol; water;

Reference yield:

: 139338-99-1
4-chloro-3-nitro-1-phenyl-1,8-naphthyridin-2(1H)-one

: 139339-08-5
1-Benzyl-5-phenyl-1H-imidazo[4,5-c][1,8]naphthyridin-4(5H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / H₂O; tetrahydrofuran / 0.5 h / Ambient temperature

2: sodium hydrosulfite / ethanol; H₂O / 0.17 h / 80 °C

3: 1 h / Heating

With sodium disulfite; In tetrahydrofuran; ethanol; water;