3-Acetylamino-2-ethyl-4(3H)-quinazolinone

Base Information

Chemical Name:3-Acetylamino-2-ethyl-4(3H)-quinazolinone
CAS No.:6761-24-6
Molecular Formula:C₁₂H₁₃N₃O₂
Molecular Weight:231.254
Hs Code.:
DSSTox Substance ID:DTXSID80445091
Nikkaji Number:J658.319I

Synonyms:6761-24-6;N-(2-Ethyl-4-oxoquinazolin-3(4H)-yl)acetamide;3-ACETYLAMINO-2-ETHYL-4(3H)-QUINAZOLINONE;DTXSID80445091;N-(2-ethyl-4-oxo-3,4-dihydroquinazolin-3-yl)acetamide;N-(2-Ethyl-4-oxo-3,4-dihydroquinazoline-3-yl)acetamide

Suppliers and Price of 3-Acetylamino-2-ethyl-4(3H)-quinazolinone

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of 3-Acetylamino-2-ethyl-4(3H)-quinazolinone

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:231.100776666
Heavy Atom Count:17
Complexity:365

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1=NC2=CC=CC=C2C(=O)N1NC(=O)C

Technology Process of 3-Acetylamino-2-ethyl-4(3H)-quinazolinone

There total 1 articles about 3-Acetylamino-2-ethyl-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:

: 16347-87-8
3-(acetylamino)-4(3H)-quinazolinone

: 74-88-4
methyl iodide

: 6761-05-3
N-(2-methyl-4-oxoquinazolin-4(3H)-yl)acetamide

: 6761-24-6
3-acetylamino-2-ethylquinazolin-4(3H)-one

: 144522-58-7
3-acetylamino-2-isopropylquinazolin-4(3H)-one

Guidance literature:: With lithium diisopropyl amide; Yield given. Multistep reaction. Yields of byproduct given; 1) heptane, THF, -78 deg C, 1 h; 2) heptane, THF, -78 deg C, 4 h;
DOI:10.1021/jo950988t

Reference yield:

: 6761-24-6
3-acetylamino-2-ethylquinazolin-4(3H)-one

: (E)-But-2-enoic acid 1-phenyl-ethyl ester

: (2S,3R)-1-(2-Ethyl-4-oxo-4H-quinazolin-3-yl)-3-methyl-aziridine-2-carboxylic acid (R)-1-phenyl-ethyl ester

: (2S,3R)-1-(2-Ethyl-4-oxo-4H-quinazolin-3-yl)-3-methyl-aziridine-2-carboxylic acid (S)-1-phenyl-ethyl ester

Guidance literature:: With 1,1,1,3,3,3-hexamethyl-disilazane; In dichloromethane; at -20 - 20 ℃; for 0.416667h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;

Reference yield:

: 6761-24-6
3-acetylamino-2-ethylquinazolin-4(3H)-one

: 19321-42-7,4511-55-1
1-phenylethyl methacrylate

: (S)-1-(2-Ethyl-4-oxo-4H-quinazolin-3-yl)-2-methyl-aziridine-2-carboxylic acid (S)-1-phenyl-ethyl ester

: (S)-1-(2-Ethyl-4-oxo-4H-quinazolin-3-yl)-2-methyl-aziridine-2-carboxylic acid (R)-1-phenyl-ethyl ester

Guidance literature:: With 1,1,1,3,3,3-hexamethyl-disilazane; In dichloromethane; at -20 - 20 ℃; for 0.416667h; Yield given. Yields of byproduct given;