TY - JOUR
T1 - Synthesis and antibacterial activity of 6-amino-2-[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]-3,4-dihydroquinazolin-4-one and its intermediate compounds
AU - Arrahman, Arif
AU - Hayun, null
AU - Suryadi, Herman
PY - 2016
Y1 - 2016
N2 - 6-Amino-2-[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]-3,4-dihydroquinazolin-4-one was synthesized in four steps. The synthesized product from each step was purified by washing and recrystallization. Purity testing was performed by examining the melting range and by thin layer chromatography. The molecular mass of the synthesized compound was determined using LC-MS. Structure of synthesized compound was elucidated using UV-visible, FT-IR, 1H NMR, 13C NMR, COSY, HMQC and HMBC. Screening for antibacterial activity was performed against Staphylococcus aureus ATCC 25923, Salmonella typhimurium ATCC 14028 and Escherichia coli ATCC 25922. The results indicated that the titled compound had been successfully synthesized and purified. The structure of desired compound was confirmed based on structural elucidation analysis. The result of testing the titled compound for the antibacterial activity was negative.
AB - 6-Amino-2-[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]-3,4-dihydroquinazolin-4-one was synthesized in four steps. The synthesized product from each step was purified by washing and recrystallization. Purity testing was performed by examining the melting range and by thin layer chromatography. The molecular mass of the synthesized compound was determined using LC-MS. Structure of synthesized compound was elucidated using UV-visible, FT-IR, 1H NMR, 13C NMR, COSY, HMQC and HMBC. Screening for antibacterial activity was performed against Staphylococcus aureus ATCC 25923, Salmonella typhimurium ATCC 14028 and Escherichia coli ATCC 25922. The results indicated that the titled compound had been successfully synthesized and purified. The structure of desired compound was confirmed based on structural elucidation analysis. The result of testing the titled compound for the antibacterial activity was negative.
KW - 6-Amino-2-[(E)-(4-hydroxy-3-methoxyphenyl)ethenyl]quinazolinone
KW - Antibacterial activity
KW - Quinazolinone
KW - Synthesis
UR - http://www.scopus.com/inward/record.url?scp=84954131404&partnerID=8YFLogxK
U2 - 10.14233/ajchem.2016.19129
DO - 10.14233/ajchem.2016.19129
M3 - Article
AN - SCOPUS:84954131404
SN - 0970-7077
VL - 28
SP - 256
EP - 260
JO - Asian Journal of Chemistry
JF - Asian Journal of Chemistry
IS - 2
ER -