Cross-condensation of derivatives of cyanoacetic acid and carbonyl compounds. Part 1: Single-stage synthesis of 1′-substituted 6-amino-spiro-4-(piperidine-4′)-2H,4H-pyrano[2,3-c]pyrazole-5-carbonitriles
✍ Scribed by Anatoliy M Shestopalov; Yuliya M Emeliyanova; Aleksandr A Shestopalov; Lyudmila A Rodinovskaya; Zukhra I Niazimbetova; Dennis H Evans
- Book ID
- 104205711
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 156 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
To develop a method of synthesis of the potentially physiologically active compounds, 1 0 -substituted 6-amino-spiro-4-(piperidine-4 0 )-2H,4H-pyrano[2,3-c]pyrazoles, we studied the three-component condensation of substituted piperidin-4-ones, malononitrile and pyrazolin-5-ones. It was found that the electrochemical method of synthesis is more regioselective, the products of the reaction are analytically pure and do not require further recrystallization.
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