Copper-Catalyzed Intramolecular α-C–H Amination via Ring-Opening Cyclization Strategy to Quinazolin-4-ones: Development and Application in Rutaecarpine Synthesis

Patel, Srilaxmi M and Biswal, Sonali and Sharada, D S and et al, . (2019) Copper-Catalyzed Intramolecular α-C–H Amination via Ring-Opening Cyclization Strategy to Quinazolin-4-ones: Development and Application in Rutaecarpine Synthesis. Synthesis, 51 (16). pp. 3160-3170. ISSN 0039-7881

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Abstract

A copper-catalyzed intramolecular α-C-H amination has been developed for the synthesis of quinazolin-4(3 H)-one derivatives from commercially available isatoic anhydride and primary and secondary benzylamines via ring-opening cyclization (ROC). This method shows good functional group tolerance and allows access to a range of 2-aryl, 2-alkyl, and spiroquinazolinone derivatives. However, 2-methylquinazolin-4(3 H)-one was synthesized from 2-amino- N -isopropylbenzamide by C-C bond cleavage, and N -benzyl-2-(methylamino)benzamide afforded 1-methyl-2-phenylquinazolin-4(1 H)-one along with 2-phenylquinazolin-4(3 H)-one by N-C bond cleavage for aromatization. It is the first general method to construct the potentially useful 2-methylquinazolin-4(3 H)-one by copper-catalyzed intramolecular C-H amination. Also this ROC strategy has been successfully applied to the synthesis of quinazolinone alkaloid rutaecarpine.

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IITH Creators:
IITH CreatorsORCiD
Sharada, D SUNSPECIFIED
Item Type: Article
Uncontrolled Keywords: 2-methylquinazolin-4(3 H)-one, intramolecular C-H amination, quinazolin-4(3 H)-one, ring-opening cyclization, rutaecarpine
Subjects: Chemistry
Divisions: Department of Chemistry
Depositing User: Team Library
Date Deposited: 19 Aug 2019 09:34
Last Modified: 19 Aug 2019 09:34
URI: http://raiith.iith.ac.in/id/eprint/5951
Publisher URL: http://doi.org/10.1055/s-0037-1611575
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