High Yielding, Base Catalyzed C6 Regioselective Amination and N9 Alkylation in Purine Nucleotide

Author:

Dhuda Gautamkumar1,Kapadiya Khushal2,Ladwa Paresh1,Godhaniya Bhavna1,Modha Jayesh1

Affiliation:

1. Department of Chemistry, Maharshi Dayanand Science College (Affilated to Bhakta Kavi Narsinh Mehta University), Porbandar-360575, India

2. Department of Chemistry, B.R.C.C. Laboratory, School of Science, R K University, Rajkot-360020, India

Abstract

2,6-Dichloropurine is an interesting new nucleoside which gave regioselectively various 2-derivatized or 6-derivatized purines by using a secondary amines. An efficient, simple and regioselective synthesis of C6 morpholine, N9 alkylated purine nucleoside derivatives were attained via chloro-amine coupling reaction between 2,6-dichloropurine with morpholine followed by commercial alkylation method using DMF and K2CO3. Over the traditionally used protocols and procedure, it have been exhibited advance benefits such as admirable yield, simple reaction conditions and modest influence.

Publisher

Asian Journal of Chemistry

Subject

General Chemistry

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