1313199-48-2Relevant articles and documents
Catalyst-free grinding method: a new avenue for synthesis of 6-amino-3-methyl-4-aryl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile and DFT studies on the mechanistic pathway of this category of compounds
Nikpassand, Mohammad,Fekri, Leila Zare,Rahro, Parissa Naddaf
, p. 1707 - 1719 (2019/01/08)
A novel, efficient, one-pot, catalyst-free grinding procedure for synthesis of 6-amino-3-methyl-4-aryl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile is reported. The condensation of substituted?benzaldehydes, 3-amino-5-methylpyrazole, and malononitrile accord
Convenient ultrasound-promoted regioselective synthesis of fused 6-amino-3-methyl-4-aryl-1h-pyrazolo[3,4-B]pyridine-5-carbonitrile
Zare, Leila,Mahmoodi, Nosrat O.,Yahyazadeh, Asieh,Mamaghani, Manouchehr
, p. 2323 - 2330 (2011/07/07)
A multicomponent, catalyst-free reaction for the synthesis of fused 6-amino-3- methyl-4-aryl-1H-pyrazolo [3,4-b] pyridine-5-carbonitrile from 3-amino-5-methylpyrazole, malononitrile, and substituted aldehydes under ultrasound irradiation in short reaction times (8-10 min) with good yields (85-98%) is reported. Copyright