(+/-)-(R*R*)-BIS-[6,7-DIMETHOXY-1-(2-CHLOROPHENYL)-3,4-DIHYDROISOQUINOLIN-2(1H)-YL]-METHANONE
Compound with spectra: 1 NMR
![(+/-)-(R*R*)-BIS-[6,7-DIMETHOXY-1-(2-CHLOROPHENYL)-3,4-DIHYDROISOQUINOLIN-2(1H)-YL]-METHANONE](/api/compound/B1w9x8vekly.png?ph=true&h=300&w=458 "(+/-)-(R*R*)-BIS-[6,7-DIMETHOXY-1-(2-CHLOROPHENYL)-3,4-DIHYDROISOQUINOLIN-2(1H)-YL]-METHANONE")
| SpectraBase Compound ID | B1w9x8vekly |
|---|---|
| InChI | InChI=1S/C35H34Cl2N2O5/c1-41-29-17-21-13-15-38(33(25(21)19-31(29)43-3)23-9-5-7-11-27(23)36)35(40)39-16-14-22-18-30(42-2)32(44-4)20-26(22)34(39)24-10-6-8-12-28(24)37/h5-12,17-20,33-34H,13-16H2,1-4H3/t33-,34-/m0/s1 |
| InChIKey | MNPBKGIEHGWVLP-HEVIKAOCSA-N |
| Mol Weight | 633.6 g/mol |
| Molecular Formula | C35H34Cl2N2O5 |
| Exact Mass | 632.184478 g/mol |
| Enantiomer InChIKey | MNPBKGIEHGWVLP-KKLWWLSJSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2(1H)-isoquinolinecarboxamide, N-(4-chlorophenyl)-1-(2-fluorophenyl)-3,4-dihydro-6,7-dimethoxy-
2,3-Dimethoxy-5,12b-dihydroisoindolo[1,2-a]isoquinolin-8(6H)-one
(+/-)-ETHYL-1-(2,4-DIMETHOXYPHENYL)-6,7-DIMETHOXY-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE
11,12-Dimethoxy-6-methyl-8,9-dihydro-6H,13bH-isoquino-2,1-c[1,3]benzoxazine
(+/-)-ETHYL-6,7-DIMETHOXY-1-(2,4,5-TRIMETHOXYPHENYL)-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE
3-CHLORO-12,13-DIMETHOXY-5,9,10,14b-TETRAHYDROISOQUINO[2,1-d][1,4]BENZODIAZEPIN-6(7H)-ONE
5,6,7,9,10,11,15B,15C-OCTAHYDRODIISOQUINOLINO-[2,1-C:1',2'-E]-IMIDAZOL-8-ONE
Octahydro-diisoquinolino[2,11-c : 1',2'-e]imidazol-8-one
8,9-Dimethoxy-1,2,3,5,6,10b-hexahydrobenzo[5,6][1,4]diazepino[7,1-a]isoquinolin-2-one
Moexipril-M/artifact 3ME @
| Title | Journal or Book | Year |
|---|---|---|
| One-Pot α-Amidosulfone-Mediated Variation of the Pictet-Spengler Tetrahydroisoquinoline Synthesis, Suitable for Amide-Type Substrates | European Journal of Organic Chemistry | 2014 |