3.8 Article

Efficient and Convenient Synthesis of Pyrrolo[1,2-a]quinazoline Derivatives with the Aid of Tin(II) Chloride

Journal

JOURNAL OF COMBINATORIAL CHEMISTRY
Volume 12, Issue 4, Pages 582-586

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cc100062e

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Funding

  1. Foundation of Key Laboratory of Organic Synthesis of Jiangsu Province

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An efficient, convenient, one-pot synthesis of 2,3,3a,4-tetrahydropyrrolo[1,2-a]quinazolin-5(1H)-one and 2,3,3a,4-tetrahydropyrrolo[1,2-a]quinazoline-1,5-dione was accomplished in good yields via the novel reductive cyclization of 2-nitrobenzamides with haloketones or keto acids mediated by SnCl2 center dot 2H(2)O system. A variety of substrates can participate in the process with good yields, making this methodology suitable for library synthesis in drug discovery efforts.

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