2-Benzylsulfanyl-3-ethylquinazolin-4-one

Base Information

Chemical Name:2-Benzylsulfanyl-3-ethylquinazolin-4-one
CAS No.:90852-43-0
Molecular Formula:C17H16N2OS
Molecular Weight:0.00000
Hs Code.:
DSSTox Substance ID:DTXSID201331820
ChEMBL ID:CHEMBL1709755
Mol file:90852-43-0.mol

Synonyms:2-benzylsulfanyl-3-ethylquinazolin-4-one;2-(benzylsulfanyl)-3-ethyl-4(3H)-quinazolinone;90852-43-0;Cambridge id 5728037;Oprea1_289588;Oprea1_617397;MLS001178547;CHEMBL1709755;DTXSID201331820;HMS2778H13;STL356494;AKOS000547499;SMR000476468;2-(benzylsulfanyl)-3-ethylquinazolin-4(3H)-one;AB00094884-01;AJ-292/11720084

Suppliers and Price of 2-Benzylsulfanyl-3-ethylquinazolin-4-one

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-Benzylsulfanyl-3-ethylquinazolin-4-one

Chemical Property:

PSA：0.00000
LogP:0.00000
XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:296.09833431
Heavy Atom Count:21
Complexity:404

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCN1C(=O)C2=CC=CC=C2N=C1SCC3=CC=CC=C3

Technology Process of 2-Benzylsulfanyl-3-ethylquinazolin-4-one

There total 4 articles about 2-Benzylsulfanyl-3-ethylquinazolin-4-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: 90.0%

: 6344-77-0
2-(benzylsulfanyl)quinazolin-4(3H)-one

: 75-03-6
ethyl iodide

: 90852-43-0
C₁₇H₁₆N₂OS

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;
DOI:10.3987/COM-12-12477

Reference yield:

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 90852-43-0
C₁₇H₁₆N₂OS

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / 2 h / Reflux

2: 0.5 h / 20 °C

3: potassium hydroxide / ethanol / 0.5 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C

With thionyl chloride; potassium carbonate; potassium hydroxide; In ethanol; N,N-dimethyl-formamide;
DOI:10.3987/COM-12-12477

Reference yield:

: 21563-73-5
2-aminobenzoyl chloride

: 90852-43-0
C₁₇H₁₆N₂OS

Guidance literature:: Multi-step reaction with 3 steps

1: 0.5 h / 20 °C

2: potassium hydroxide / ethanol / 0.5 h / 20 °C

3: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C

With potassium carbonate; potassium hydroxide; In ethanol; N,N-dimethyl-formamide;
DOI:10.3987/COM-12-12477