6,7-DIMETHOXY-3-METHYL-1-(4-METHYLPHENYL)-2-[5-[3-[4-(2-PYRIMIDINYL)-PIPERAZIN-1-YL]-PROPYLTHIO]-1,2,4-TRIAZOL-3-YL]-1,2-DIHYDROISOQUINOLINE
Compound with spectra: 1 NMR
![6,7-DIMETHOXY-3-METHYL-1-(4-METHYLPHENYL)-2-[5-[3-[4-(2-PYRIMIDINYL)-PIPERAZIN-1-YL]-PROPYLTHIO]-1,2,4-TRIAZOL-3-YL]-1,2-DIHYDROISOQUINOLINE](/api/compound/FiezLBr0MPU.png?ph=true&h=300&w=458 "6,7-DIMETHOXY-3-METHYL-1-(4-METHYLPHENYL)-2-[5-[3-[4-(2-PYRIMIDINYL)-PIPERAZIN-1-YL]-PROPYLTHIO]-1,2,4-TRIAZOL-3-YL]-1,2-DIHYDROISOQUINOLINE")
| SpectraBase Compound ID | FiezLBr0MPU |
|---|---|
| InChI | InChI=1S/C32H38N8O2S/c1-22-7-9-24(10-8-22)29-26-21-28(42-4)27(41-3)20-25(26)19-23(2)40(29)31-35-32(37-36-31)43-18-6-13-38-14-16-39(17-15-38)30-33-11-5-12-34-30/h5,7-12,19-21,29H,6,13-18H2,1-4H3,(H,35,36,37) |
| InChIKey | DZCSOWVHXRRDQM-UHFFFAOYSA-N |
| Mol Weight | 598.8 g/mol |
| Molecular Formula | C32H38N8O2S |
| Exact Mass | 598.283844 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
6,7-DIMETHOXY-3-METHYL-1-(4-METHYLPHENYL)-2-[5-[3-(N,N-DIMETHILAMINO)-PROPYLTHIO]-1,2,4-TRIAZOL-3-YL]-1,2-DIHYDROISOQUINOLINE
6,7-DIMETHOXY-3-METHYL-1-(4-METHYLPHENYL)-2-(5-ETHYLTHIO-1,2,4-TRIAZOL-3-YL)-1,2-DIHYDROISOQUINOLINE
6,7-DIMETHOXY-3-METHYL-1-(4-NITROPHENYL)-2-(PYRAZOL-3-YL)-1,2-DIHYDROISOQUINOLINE
(+-)-Trans-2,3-methylenedioxy-11-methyl-6a,12b-dihydro-6H-chromeno[3,4-c]isoquinolin-8-one
11-(3,4-Dimethoxyphenyl)-3,3,7,8-tetramethyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one
CUMAMBRANOLIDE,8-B-ACETYLSARRACIONYLOXY
1-Anthracenesulfonamide, 9,10-dihydro-5-nitro-9,10-dioxo-N-[2-(3-pentadecylphenoxy)butyl]-
1-Phenyl-3-(3-pyridinyl)spiro[aziridine-2,9'-fluorene]
ETHYL-3-ISOBUTYL-2,5-DIOXO-2,3-DIHYDRO-5H-PYRROLO-[1,2-A]-ISOINDOLE-1-CARBOXYLATE
(3AR,6S,7R,8S,9AR)-7,8,9-TRI-(BENZYLOXY)-6-TERT.-BUTYLDIMETHYLSILYLOXY-OCTAHYDRO-CYCLOOCTAOXAZOL-2-ONE
| Title | Journal or Book | Year |
|---|---|---|
| Unexpected formation of 1,2-dihydro-2-azolyl-and azinylisoquinolines by the reduction of the corresponding isoquinolinium salts with sodium borohydride in methanol | Journal of Heterocyclic Chemistry | 2004 |