4.4 Article

An Efficient Protocol for the Synthesis of Pyrazolo[1,5-c]quinazolines by a Staudinger-Aza-Wittig-Dehydroaromatization Sequence

期刊

SYNLETT
卷 32, 期 18, 页码 1874-1878

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/a-1579-1692

关键词

azidodihydropyrazoles; aza-Wittig reaction; Staudinger reaction; cascade reaction; dehydroaromatization; pyrazoloquinazolines

资金

  1. Key Project of Hubei Educational Committee [D20182602]
  2. Doctoral Startup Foundation of Hubei University of Arts and Science
  3. Student Innovation Training Program [X202110519136]

向作者/读者索取更多资源

The one-pot synthesis of azide-substituted dihydropyrazoles in isopropanol was successfully achieved, followed by investigation of Staudinger-aza-Wittig-dehydroaromatization reactions with methyl(diphenyl)phosphine for further application in the construction of pyrazolo[1,5- c ]quinazolines.
The one-pot synthesis of azide-substituted dihydropyrazoles in isopropanol was performed by using chalcones, hydrazine hydrate, and an acyl chloride at 0 celcius. Subsequent Staudinger-aza-Wittig-dehydroaromatization reactions of the products with methyl(diphenyl)phosphine were also investigated for further application in the construction of pyrazolo[1,5- c ]quinazolines.

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