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DOI: 10.1055/s-0032-1318107
Synthesis of Tetrahydropyrazolo[1,5-c]pyrimidine-2,7(1H,3H)-diones
Publication History
Received: 22 November 2012
Accepted after revision: 27 December 2012
Publication Date:
24 January 2013 (online)
![](https://www.thieme-connect.de/media/synthesis/201305/lookinside/thumbnails/10.1055-s-0032-1318107-1.jpg)
Dedicated to Professor Emeritus Volker Jäger, Institut für Organische Chemie, Universität Stuttgart, on the occasion of his 70th birthday.
Abstract
A series of tetrahydropyrazolo[1,5-c]pyrimidine-2,7(1H,3H)-diones 3a–h as the first representatives of the so far unexplored saturated heterocyclic system have been synthesized, formally in 12 steps from methyl acrylate (4). The synthesis comprises a four-step preparation of methyl N-Cbz-5-alkylamino-3-oxopentanoates 9a–c, their three-step transformation into 5-{2-[(alkyl)(benzyloxycarbonyl)amino]ethyl}pyrazolidin-3-ones 12a–c, three-step selective alkylation of the amidic N-2 to give 2-alkyl-5-{2-[(alkyl)(benzyloxycarbonyl)amino]ethyl}pyrazolidin-3-ones 16b–h, followed by hydrogenolytic Cbz-deprotection and subsequent cyclization of the intermediate 1,4-diamine with CDI to furnish the title compounds 3. Most of the synthetic steps were performed as a one-pot transformation.
Supporting Information
- for this article containing copies of 1H and 13C spectra of compounds 3, 8–13, 15, and 16 is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
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