3-Butyl-4-ethoxy-1-phenyl-1,8-naphthyridin-2(1H)-one

Base Information

Chemical Name:3-Butyl-4-ethoxy-1-phenyl-1,8-naphthyridin-2(1H)-one
CAS No.:89108-86-1
Molecular Formula:C20H22N2O2
Molecular Weight:322.407
Hs Code.:
ChEMBL ID:CHEMBL303417
DSSTox Substance ID:DTXSID80557582
Wikidata:Q82439532

Synonyms:89108-86-1;3-Butyl-4-ethoxy-1-phenyl-1,8-naphthyridin-2(1H)-one;CHEMBL303417;DTXSID80557582

Suppliers and Price of 3-Butyl-4-ethoxy-1-phenyl-1,8-naphthyridin-2(1H)-one

Supply Marketing:

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

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Chemical Property of 3-Butyl-4-ethoxy-1-phenyl-1,8-naphthyridin-2(1H)-one

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:322.168127949
Heavy Atom Count:24
Complexity:468

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC1=C(C2=C(N=CC=C2)N(C1=O)C3=CC=CC=C3)OCC

Technology Process of 3-Butyl-4-ethoxy-1-phenyl-1,8-naphthyridin-2(1H)-one

There total 5 articles about 3-Butyl-4-ethoxy-1-phenyl-1,8-naphthyridin-2(1H)-one 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: 60.0%

: 89109-20-6
3-(n-butyl)-4-hydroxy-1-phenyl-1,8-naphthyridine-2(1H)-one

: 89108-86-1
3-Butyl-4-ethoxy-1-phenyl-1H-[1,8]naphthyridin-2-one

Guidance literature:: With potassium carbonate; In acetone; Heating; 1.) 0.5 h, 2.) 24 h;
DOI:10.1021/jm00119a010

Reference yield:

: 40134-18-7
methyl 2-chloropyridine-3-carboxylate

: 89108-86-1
3-Butyl-4-ethoxy-1-phenyl-1H-[1,8]naphthyridin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent

2: 80 percent / potassium tert-butoxide / 1.) 0.25 h, 2.) heating, 4 h

3: 60 percent / 1.) potassium carbonate / acetone / Heating; 1.) 0.5 h, 2.) 24 h

With potassium tert-butylate; potassium carbonate; In acetone;
DOI:10.1021/jm00119a010

Reference yield:

: 51269-84-2
methyl 2-phenylamino-nicotinate

: 89108-86-1
3-Butyl-4-ethoxy-1-phenyl-1H-[1,8]naphthyridin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / potassium tert-butoxide / 1.) 0.25 h, 2.) heating, 4 h

2: 60 percent / 1.) potassium carbonate / acetone / Heating; 1.) 0.5 h, 2.) 24 h

With potassium tert-butylate; potassium carbonate; In acetone;
DOI:10.1021/jm00119a010