2-(1-Ethylpropyl)-3-(2-methylphenyl)-4(3H)-quinazolinone

Base Information

Chemical Name:2-(1-Ethylpropyl)-3-(2-methylphenyl)-4(3H)-quinazolinone
CAS No.:73323-95-2
Molecular Formula:C₂₀H₂₂N₂O
Molecular Weight:306.407
Hs Code.:
DSSTox Substance ID:DTXSID901199059

Synonyms:2-(1-Ethylpropyl)-3-(2-methylphenyl)-4(3H)-quinazolinone;DTXSID901199059;73323-95-2

Suppliers and Price of 2-(1-Ethylpropyl)-3-(2-methylphenyl)-4(3H)-quinazolinone

Supply Marketing:

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

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Chemical Property of 2-(1-Ethylpropyl)-3-(2-methylphenyl)-4(3H)-quinazolinone

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:306.173213330
Heavy Atom Count:23
Complexity:455

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC(CC)C1=NC2=CC=CC=C2C(=O)N1C3=CC=CC=C3C

Technology Process of 2-(1-Ethylpropyl)-3-(2-methylphenyl)-4(3H)-quinazolinone

There total 2 articles about 2-(1-Ethylpropyl)-3-(2-methylphenyl)-4(3H)-quinazolinone 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: 42.0%

: 73308-59-5
C₁₆H₁₃LiN₂O

: 75-03-6
ethyl iodide

: 72-44-6
methaqualone

: 30006-43-0
2-propyl-3-o-tolyl-3H-quinazolin-4-one

: 73323-95-2
2-(3-pentyl)-3-o-tolyl-4(3H)-quinazolinone

Guidance literature:: With diisopropylamine; In tetrahydrofuran; hexane; for 1h;
DOI:10.1021/jo01299a027

Reference yield:

: 72-44-6
methaqualone

: 73323-95-2
2-(3-pentyl)-3-o-tolyl-4(3H)-quinazolinone

Guidance literature:: Multi-step reaction with 2 steps

1: diisopropylamine, n-butyllithium / tetrahydrofuran; hexane / 0.58 h

2: 5 percent / diisopropylamine / tetrahydrofuran; hexane / 1 h

With n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane;
DOI:10.1021/jo01299a027