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Molecular iodine-catalyzed combinatorial library synthesis of 2-amino-3-cyano-4H-pyran derivatives at ambient temperature

Publish Year: 1397
Type: Journal paper
Language: English
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Document National Code:

JR_CIC-1-2_002

Index date: 25 May 2019

Molecular iodine-catalyzed combinatorial library synthesis of 2-amino-3-cyano-4H-pyran derivatives at ambient temperature abstract

An efficient and simple synthesis of some 2-amino-3-cyano-4H-pyran derivatives was developed via the one-pot and three-component reaction of aldehydes, ethyl acetoacetate, and malononitrile in the presence of ammonium acetate at room temperature using catalytic amount of iodine. The key advantages of this method are the easy access to various substituted 2-amino-3-cyano-4H-pyran derivatives, short reaction times and high yields.

Molecular iodine-catalyzed combinatorial library synthesis of 2-amino-3-cyano-4H-pyran derivatives at ambient temperature Keywords:

Molecular iodine-catalyzed combinatorial library synthesis of 2-amino-3-cyano-4H-pyran derivatives at ambient temperature authors

Adeleh Moshtaghi Zonouz

Chem. Dep., Fac. Sci, Azarbaijan Shahid Madani Univ., Tabriz, Iran

Saeed Behjat

Naft research center