Acetamide, N-(2-(4-(4-morpholinyl)-3-nitrophenyl)-4-oxo-3(4H)-quinazolinyl)-2-(4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)-

Base Information

Chemical Name:Acetamide, N-(2-(4-(4-morpholinyl)-3-nitrophenyl)-4-oxo-3(4H)-quinazolinyl)-2-(4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)-
CAS No.:136603-30-0
Molecular Formula:C₄₁H₃₁N₇O₇
Molecular Weight:733.74
Hs Code.:
DSSTox Substance ID:DTXSID30159853
Wikidata:Q83028230
Mol file:136603-30-0.mol

Synonyms:BRN 4900543;136603-30-0;Acetamide, N-(2-(4-(4-morpholinyl)-3-nitrophenyl)-4-oxo-3(4H)-quinazolinyl)-2-(4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)-;DTXSID30159853;C41H31N7O7;C41-H31-N7-O7

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Chemical Property of Acetamide, N-(2-(4-(4-morpholinyl)-3-nitrophenyl)-4-oxo-3(4H)-quinazolinyl)-2-(4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：177.85000
Density:1.43g/cm³
LogP:7.03630
XLogP3:5.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:8
Exact Mass:733.22849635
Heavy Atom Count:55
Complexity:1410

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1COCCN1C2=C(C=C(C=C2)C3=NC4=CC=CC=C4C(=O)N3NC(=O)COC5=CC=C(C=C5)C(=O)C6=C(N=C7C(=C6)C=CC=N7)C8=CC=CC=C8)[N+](=O)[O-]

Technology Process of Acetamide, N-(2-(4-(4-morpholinyl)-3-nitrophenyl)-4-oxo-3(4H)-quinazolinyl)-2-(4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)-

There total 6 articles about Acetamide, N-(2-(4-(4-morpholinyl)-3-nitrophenyl)-4-oxo-3(4H)-quinazolinyl)-2-(4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)- 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:

: 7521-41-7
2-Aminonicotinaldehyde

: 136603-30-0
N-[2-(4-Morpholin-4-yl-3-nitro-phenyl)-4-oxo-4H-quinazolin-3-yl]-2-[4-(2-phenyl-[1,8]naphthyridine-3-carbonyl)-phenoxy]-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: conc. H₂SO₄, glac. AcOH

2: 65 percent / K₂CO₃ / acetone / 18 h / Heating

3: 60 percent / hydrazine hydrate / methanol / 8 h / Heating

4: 60 percent / 1) heating, 2 min, 2) CH₃OH, r.t., overnight

5: pyridine / 24 h / Heating

With pyridine; sulfuric acid; potassium carbonate; hydrazine hydrate; acetic acid; In methanol; acetone;

Reference yield:

: 52046-71-6
1-(4-hydroxy-phenyl)-3-phenyl-propane-1,3-dione

: 136603-30-0
N-[2-(4-Morpholin-4-yl-3-nitro-phenyl)-4-oxo-4H-quinazolin-3-yl]-2-[4-(2-phenyl-[1,8]naphthyridine-3-carbonyl)-phenoxy]-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: conc. H₂SO₄, glac. AcOH

2: 65 percent / K₂CO₃ / acetone / 18 h / Heating

3: 60 percent / hydrazine hydrate / methanol / 8 h / Heating

4: 60 percent / 1) heating, 2 min, 2) CH₃OH, r.t., overnight

5: pyridine / 24 h / Heating

With pyridine; sulfuric acid; potassium carbonate; hydrazine hydrate; acetic acid; In methanol; acetone;

Reference yield:

: 116625-85-5
3-p-Hydroxybenzoyl-2-phenyl-1,8-naphthyridine

: 136603-30-0
N-[2-(4-Morpholin-4-yl-3-nitro-phenyl)-4-oxo-4H-quinazolin-3-yl]-2-[4-(2-phenyl-[1,8]naphthyridine-3-carbonyl)-phenoxy]-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 65 percent / K₂CO₃ / acetone / 18 h / Heating

2: 60 percent / hydrazine hydrate / methanol / 8 h / Heating

3: 60 percent / 1) heating, 2 min, 2) CH₃OH, r.t., overnight

4: pyridine / 24 h / Heating

With pyridine; potassium carbonate; hydrazine hydrate; In methanol; acetone;