An expeditious synthesis of 2-aryl- and 2-alkylquinazolin-4(3H)-ones

DOI: 10.1055/s-1991-26632

Source and publish data:

Synthesis p. 1009 - 1010 (1991)

Update date:2022-08-11

Topics:

Authors:

Couture Couture

Cornet Cornet

Grandclaudon

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1055/s-1991-26632

2-Aryl- and alkylquinazolin-4(3H)-ones are readily accessible by reaction of the lithium 2-(diethylaminocarbonyl)anilide with appropriate aryl and alkyl nitriles.

Full text of DOI:10.1055/s-1991-26632

Products guided by the article

Product name:2-PHENYL-4-[3H]QUINAZOLINONE

Cas No:1022-45-3

R&D Labs maybe for 1022-45-3

ShangHai Original Economy-Trade Develop Co.,Ltd.,

Contact:86-21-68552131

Address:shanghai
ShangHai Ruiyi Medical Technology Co.,Ltd.

Contact:+86-21-54718086

Address:No951 Jianchuan RD，Minhang District
Hefei Highzone Fine Chemical S&T CO.,LTD

Contact:86-0551-63663560

Address:room 1801 NO. 24 Shuguang RD.
ClickChem Technology Co., Limited

Contact:+86-0310-6519966/0531-52893837

Address:No.750 Shunhua Road, High-Tech Zone, Jinan city, Shandong China
Career Henan Chemical Co

website:http://www.coreychem.com

Contact:+86-371-86658258

Address:Building 10 of Innovation Park, East District of the National University Science Park

Relevant to this article

Mechanisms for the effects of fluorine and α-diimine backbone structure on the catalyst behavior and catalyst deactivation in ethylene polymerization by Ni catalysts

Doi:10.1016/j.jorganchem.2017.02.043
(2017)
A new tetradentate mixed aza-thioether macrocycle and its complexation behavior towards Fe(II), Ni(II) and Cu(II) ions

Doi:10.3390/molecules25092030
(2020)
Doi:10.1016/S0022-328X(00)87415-X
(1971)
Doi:10.1039/jr9560003121
(1956)
Stereochemistry of Endogenous Palmitic Acid Ester of 9-Hydroxystearic Acid and Relevance of Absolute Configuration to Regulation

Doi:10.1021/jacs.7b01269
(2017)
Kinetics and mechanistic studies on the formation and reactivity of high valent MnO porphyrin species: Mono-: ortho or para -substituted porphyrins versus a di- ortho -substituted one

Doi:10.1039/c7nj04233g
(2018)

Article Doi