TY - JOUR
T1 - One-pot four-component synthesis of phenazine derivative using 2-hydroxy-1,4-naphthoquinone
AU - Cahyana, A. H.
AU - Nazhifah, N.
AU - Liandi, A. R.
N1 - Publisher Copyright:
© Published under licence by IOP Publishing Ltd.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020
Y1 - 2020
N2 - Phenazine is one of the most important organic compounds because of its various biological activities. This study aims to synthesize the phenazine derivatives compound using 2-hydroxy-1,4-naphthoquinone (lawsone) with a one-pot four-component method.Phenazine derivative that had been successfully synthesized was carried out by reacting four reactants at once in one flask with the same mole ratio. The reaction occurred between lawsone, o-phenylenediamine, benzaldehyde, and malononitrile. Characterization of the synthesized products was confirmed using FT-IR, UV-Vis Spectrophotometer, and LC-MS. The results of the analysis using several of these instruments obtained one compound, namely 3-amino-2-cyano-1-phenyl-1H-benzo[a]pyrano[2,3-c]phenazine. The reaction conditions were carried out at 50 C for 6 h in ethanol with unassisted catalysts and obtained a product yield of 45%.
AB - Phenazine is one of the most important organic compounds because of its various biological activities. This study aims to synthesize the phenazine derivatives compound using 2-hydroxy-1,4-naphthoquinone (lawsone) with a one-pot four-component method.Phenazine derivative that had been successfully synthesized was carried out by reacting four reactants at once in one flask with the same mole ratio. The reaction occurred between lawsone, o-phenylenediamine, benzaldehyde, and malononitrile. Characterization of the synthesized products was confirmed using FT-IR, UV-Vis Spectrophotometer, and LC-MS. The results of the analysis using several of these instruments obtained one compound, namely 3-amino-2-cyano-1-phenyl-1H-benzo[a]pyrano[2,3-c]phenazine. The reaction conditions were carried out at 50 C for 6 h in ethanol with unassisted catalysts and obtained a product yield of 45%.
UR - http://www.scopus.com/inward/record.url?scp=85096473577&partnerID=8YFLogxK
U2 - 10.1088/1757-899X/902/1/012020
DO - 10.1088/1757-899X/902/1/012020
M3 - Conference article
AN - SCOPUS:85096473577
SN - 1757-8981
VL - 902
JO - IOP Conference Series: Materials Science and Engineering
JF - IOP Conference Series: Materials Science and Engineering
IS - 1
M1 - 012020
T2 - 4th International Symposium on Current Progress in Functional Materials, ISCPFM 2019
Y2 - 6 November 2019 through 7 November 2019
ER -