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Synthesis of 5‐Cyanopyrazolo[3,4‐ B ]Pyridines in the Reaction of 5‐Amino‐3‐methyl‐1‐phenylpyrazole with Arylidene Derivatives of Malonodinitrile and Ethyl Cyanoacetate by Jairo Quiroga; Mario Alvarado; Braulio Insuasty; Rodolfo Moreno; Enrique Raviña; Isabel Estevez; Regina H. De Almeida S. is a Chemistry article available to read on EtoBox.

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## Abstract This paper describes the synthesis of a new series of 6‐amino‐4‐aryl‐5‐cyanopyrazolo[3,4‐__b__]pyridines 4 and 4‐aryl‐5‐cyano‐6__H__‐pyrazolo[3,4‐__b__]pyridin‐6‐ones 5 from the reaction of 5‐amino‐3‐methyl‐1‐phenylpyrazole 1 with arylidene derivatives of malonodinitrile 2 and ethyl cyanoacetate 3. The structure of the final compounds was determined on the basis of nmr measurements, especially by ^1^H, ^1^H‐, ^1^H, ^13^C‐COSY, DEPT and X‐ray diffraction.

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Author
Jairo Quiroga; Mario Alvarado; Braulio Insuasty; Rodolfo Moreno; Enrique Raviña; Isabel Estevez; Regina H. De Almeida S.
Publisher
Journal of Heterocyclic Chemistry; Wiley (John Wiley & Sons); Wiley-Blackwell; Wiley; FASEB (ISSN 0022-152X)
Published
1999
Language
EN
Field
Chemistry (Physical Sciences)

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