1029475-63-5

Basic information

• Product Name: 1-amino-5-(4-methylbenzoyl)-4-(4-methylphenyl)-1H-pyrimidine-2-one
• Synonyms: 1-amino-5-(4-methylbenzoyl)-4-(4-methylphenyl)-1H-pyrimidine-2-one
• CAS NO: 1029475-63-5
• Molecular Weight: 319.363
• Mol File: 1029475-63-5.mol

Chemical Properties

• CAS DataBase Reference: 1-amino-5-(4-methylbenzoyl)-4-(4-methylphenyl)-1H-pyrimidine-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-amino-5-(4-methylbenzoyl)-4-(4-methylphenyl)-1H-pyrimidine-2-one(1029475-63-5)
• EPA Substance Registry System: 1-amino-5-(4-methylbenzoyl)-4-(4-methylphenyl)-1H-pyrimidine-2-one(1029475-63-5)

Safety Data

• Hazardous Substances Data: 1029475-63-5(Hazardous Substances Data)

Upstream product

• 3352-98-5 p-methyl acetophenone semicarbazone 

Downstream Products

• 1180548-87-1 3-(4-methoxybenzoyl)-2-(4-methoxyphenyl)-4-(4-methylbenzoyl)-5-(4-methylphenyl)-3a,6-dihydropyrazolo[1,5-c]pyrimidin-7(3H)-one 
• 1180548-90-6 3,4-bis(4-methylbenzoyl)-2,5-bis(4-methylphenyl)-3a,6-dihydropyrazolo[1,5-c]pyrimidin-7(3H)-one 
• 1180548-82-6 3-benzoyl-4-(4-methylbenzoyl)-5-(4-methylphenyl)-2-phenyl-3a,6-dihydropyrazolo[1,5-c]pyrimidin-7(3H)-one 
• 1180548-77-9 3-acetyl-4-(4-methylbenzoyl)-2-methyl-5-(4-methylphenyl)-3a,6-dihydropyrazolo-[1,5-c]pyrimidin-7(3H)-one 
• 1333503-36-8 N,N'-bis[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-oxopyrimidin-1(2H)-yl]ethanediamide 

Relevant articles and documents

Reactions of 4-(4-methylbenzoyl)-5-(4-methylphenyl)-2,3-furandione with semi/thiosemi-carbazones

The 4-(4-methylbenzoyl)-5-(4-methylphenyl)-2,3-furandione (1) and various semi-/thiosemicarbazones 2a-h combine with loss of carbondioxide and water yielding 1-methylenaminopyrimidine-2-one and -thione derivatives 3a-h, in moderate yields (43-59%). Hydrol

Reactions of aminopyrimidine derivatives with chloroacetyl and isophthaloyl chlorides

1-Aminopyrimidine-2-one derivatives (1a-c) were prepared in two steps from furan-2,3-diones and semicarbazones in toluene/benzene. Pyrimidin-[1(2H)-yl] acetamide derivatives and isophthalimide derivatives were synthesized from the nucleophilic acyl substi

Design, synthesis, in vitro antiproliferative activity properties, quantum chemical and molecular docking studies of novel Schiff bases incorporating pyrimidine nucleus

In this study, a series of new Schiff bases, based on a pyrimidine core, were synthesized by the condensation reactions of 1-amino-5-(4-methylbenzoyl)-4-p-tolylpyrimidin-2(1H)-one (1a) and 1-amino-5-(4-methylbenzoyl)-4-p-tolylpyrimidine-2(1H)-thione (1b) with different aromatic aldehyde derivatives using p-toluene sulfonic acid as a catalyst at refluxing in ethyl alcohol. The structures of these newly synthesized Schiff bases (2-11) were verified by 1H NMR, 13C NMR, IR, LC-MS (only for 2, 3, 5, 6, 8, 9, 11), and elemental analysis. The presence of characteristic peaks proving the formation of imine supports the molecules' structures. The cytotoxic effects of molecules 2-11 on the viability of breast (MDA-MB-231) and colon (DLD-1) cancer cells were investigated using the MTT method. The molecules (2-11) demonstrated in vitro antiproliferative activity in the MDA-MB-231 cell line with IC50 values ranging from 58.59 μM to ?200 μM. A compound 3 was particularly found to be the most potent anticancer drug candidate in this series with an IC50 value of 58.59 μM in MDA-MB-231. Unfortunately, neither the activity of this compound nor the others are high enough to be compared with the positive control drug cisplatin against MDA-MB-231 and DLD-1. In addition, Density Functional Theory (DFT) calculations of compounds 3, 4 and 8 were performed and the molecular docking studies of these compounds with breast cancer protein, PDB ID: 1JNX were presented to compare with experimental and theoretical results.