6-AMINO-4-BENZYL-5-CYANO-1-[4-[1-[4-(ISOPROPYLAMINO)-6-(METHYLTHIO)-1,3,5-TRIAZIN-2-YL]-1H-1,2,3-TRIAZOL-4-YL]-PHENYL]-2(1H)-PYRIMIDINONE
Compound with spectra: 1 NMR
![6-AMINO-4-BENZYL-5-CYANO-1-[4-[1-[4-(ISOPROPYLAMINO)-6-(METHYLTHIO)-1,3,5-TRIAZIN-2-YL]-1H-1,2,3-TRIAZOL-4-YL]-PHENYL]-2(1H)-PYRIMIDINONE](/api/compound/1lBBEFn8u1y.png?ph=true&h=300&w=458 "6-AMINO-4-BENZYL-5-CYANO-1-[4-[1-[4-(ISOPROPYLAMINO)-6-(METHYLTHIO)-1,3,5-TRIAZIN-2-YL]-1H-1,2,3-TRIAZOL-4-YL]-PHENYL]-2(1H)-PYRIMIDINONE")
| SpectraBase Compound ID | 1lBBEFn8u1y |
|---|---|
| InChI | InChI=1S/C27H25N11OS/c1-16(2)30-24-32-25(34-26(33-24)40-3)37-15-22(35-36-37)18-9-11-19(12-10-18)38-23(29)20(14-28)21(31-27(38)39)13-17-7-5-4-6-8-17/h4-12,15-16H,13,29H2,1-3H3,(H,30,32,33,34) |
| InChIKey | OXUWANVVHSVDFV-UHFFFAOYSA-N |
| Mol Weight | 551.63 g/mol |
| Molecular Formula | C27H25N11OS |
| Exact Mass | 551.196426 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
6-AMINO-4-BENZYL-5-CYANO-1-[3-[1-(PHENYLTHIOMETHYL)-1H-1,2,3-TRIAZOL-4-YL]-PHENYL]-2(1H)-PYRIMIDINONE
6-AMINO-5-CYANO-1-(2,3-DIHYDROBENZO-[B]-[1,4]-DIOXIN-6-YL)-4-(4-METHYLPHENYL)-2(1H)-PYRIMIDINONE
6-AMINO-5-CYANO-1-(NAPHTHALEN-1-YL)-4-PHENYL-2(1H)-PYRIMIDINONE
4-Cyclohexyl-1-(4-methylphenyl)-6-phenyl-5-propenyl-2(1H)-pyrimidone
N-(5-Chloro-2-methoxyphenyl)-2-(4-methoxyphenyl)-5-oxo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-7-carboxamide
4-[(2Z)-6-amino-5-cyano-2-ethylidene-3-methyl-4,4-bis(trifluoromethyl)-3H-pyridin-1-yl]benzamide
2H,6H-pyrido[2,1-b][1,3,5]thiadiazine-9-carbonitrile, 8-(3-bromophenyl)-3-(4-fluorophenyl)-3,4,7,8-tetrahydro-6-oxo-
ACULENE-B
tert-Butyl 6-Ethyl-2-oxo-3-phenyl-2,3-dihydro-1H-thieno[2,3-b][1,4]thiazin-1-carboxylate
Ethyl 3-acetyl-1-(4-nitrophenyl)-5-phenyl-1H-pyrazole-4-carboxylate
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of 6-Amino-5-cyano-1,4-disubstituted-2(1H)-Pyrimidinones via Copper-(I)-catalyzed Alkyne-azide ‘Click Chemistry’ and Their Reactivity | Molecules | 2010 |