TY - JOUR
T1 - Efficiency and potential synthesis of pyrimido [4,5-d] pyrimidine derivatives by iodine catalyst as antioxidant agent
AU - Cahyana, A. H.
AU - Liandi, A. R.
AU - Zaky, M. Z.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 - Pyrimido [4,5-d] pyrimidine is an uracil compound that has similarities to the structure of pteridine and purines and has significant bioactivity. The aim of this research is to synthesize pyrimido [4,5-d] pyrimidine derivatives and test their activity as antioxidant. The reaction was carried out with the support of the iodine catalyst to get an effective reaction. Experimental evidence in support of the formation products was confirmed using FTIR, UV-vis Spectrophotometer, and GC-MS. The results of the analysis produced four pyrimido [4,5-d] pyrimidine derivatives, 5-Styryl-5,8-dihydro-1H,6H-pyrimido[4,5-d]pyrimidine-2,4,7-trione (compound 1), 5-Styryl-7-thioxo-5,6,7,8-tetrahydro-1H-pyrimido[4,5-d]pyrimidine-2,4-dione (compound 2), 5-Phenyl-5,8-dihydro-1H,6H-pyrimido[4,5-d]pyrimidine-2,4,7-trione (compound 3), and 5-Phenyl-7-thioxo-5,6,7,8-tetrahydro-1H-pyrimido[4,5-d]pyrimidine-2,4-dione (compound 4). Reaction optimization was conducted by varying reaction time, reaction temperature, amount of catalyst and solvent. The optimum conditions of the reaction were obtained under conditions of 10 % mol of catalyst, temperature 70 C, for 4 h with a water solvent. Compound 1 has a better activity than 3 other compounds with an IC50 value of 10.11 ppm.
AB - Pyrimido [4,5-d] pyrimidine is an uracil compound that has similarities to the structure of pteridine and purines and has significant bioactivity. The aim of this research is to synthesize pyrimido [4,5-d] pyrimidine derivatives and test their activity as antioxidant. The reaction was carried out with the support of the iodine catalyst to get an effective reaction. Experimental evidence in support of the formation products was confirmed using FTIR, UV-vis Spectrophotometer, and GC-MS. The results of the analysis produced four pyrimido [4,5-d] pyrimidine derivatives, 5-Styryl-5,8-dihydro-1H,6H-pyrimido[4,5-d]pyrimidine-2,4,7-trione (compound 1), 5-Styryl-7-thioxo-5,6,7,8-tetrahydro-1H-pyrimido[4,5-d]pyrimidine-2,4-dione (compound 2), 5-Phenyl-5,8-dihydro-1H,6H-pyrimido[4,5-d]pyrimidine-2,4,7-trione (compound 3), and 5-Phenyl-7-thioxo-5,6,7,8-tetrahydro-1H-pyrimido[4,5-d]pyrimidine-2,4-dione (compound 4). Reaction optimization was conducted by varying reaction time, reaction temperature, amount of catalyst and solvent. The optimum conditions of the reaction were obtained under conditions of 10 % mol of catalyst, temperature 70 C, for 4 h with a water solvent. Compound 1 has a better activity than 3 other compounds with an IC50 value of 10.11 ppm.
UR - http://www.scopus.com/inward/record.url?scp=85096470730&partnerID=8YFLogxK
U2 - 10.1088/1757-899X/902/1/012039
DO - 10.1088/1757-899X/902/1/012039
M3 - Conference article
AN - SCOPUS:85096470730
SN - 1757-8981
VL - 902
JO - IOP Conference Series: Materials Science and Engineering
JF - IOP Conference Series: Materials Science and Engineering
IS - 1
M1 - 012039
T2 - 4th International Symposium on Current Progress in Functional Materials, ISCPFM 2019
Y2 - 6 November 2019 through 7 November 2019
ER -