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#9D;(+/-)-[6R*,11AS*,(3Z)]-6-(4-BROMOPHENYL)-3-(3,4-DIMETHOXYBENZYLIDENE)-8,9-DIMETHOXY-2,3,11,11A-TETRAHYDRO-1H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4-DIONE

Compound with spectra: 1 NMR

#9D;(+/-)-[6R*,11AS*,(3Z)]-6-(4-BROMOPHENYL)-3-(3,4-DIMETHOXYBENZYLIDENE)-8,9-DIMETHOXY-2,3,11,11A-TETRAHYDRO-1H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4-DIONE
SpectraBase Compound ID HXoBFMo6a1y
InChI InChI=1S/C29H27BrN2O6/c1-35-23-10-5-16(12-24(23)36-2)11-21-29(34)32-22(28(33)31-21)13-18-14-25(37-3)26(38-4)15-20(18)27(32)17-6-8-19(30)9-7-17/h5-12,14-15,22,27H,13H2,1-4H3,(H,31,33)/b21-11-/t22-,27+/m0/s1
InChIKey MOVKNIFTYATSOA-NWANQZCCSA-N
Mol Weight 579.45 g/mol
Molecular Formula C29H27BrN2O6
Exact Mass 578.10525 g/mol
Enantiomer InChIKey MOVKNIFTYATSOA-KKWCIZTPSA-N

View Spectrum of #9D;(+/-)-[6R*,11AS*,(3Z)]-6-(4-BROMOPHENYL)-3-(3,4-DIMETHOXYBENZYLIDENE)-8,9-DIMETHOXY-2,3,11,11A-TETRAHYDRO-1H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4-DIONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(+/-)-[6R*,11AS*,(3Z)]-3-(3,4-DIMETHOXYBENZYLIDENE)-6-ETHYL-8,9-DIMETHOXY-2,3,11,11A-TETRAHYDRO-6H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4-DIONE
(+/-)-[6R*,11AS*,(3Z)]-3-(3,4-DIMETHOXYBENZYLIDENE)-8,9-DIMETHOXY-6-PROPYL-2,3,11,11A-TETRAHYDRO-6H-PYRAZINO-[1,2-B]-ISOQUINOLINE-1,4-DIONE
(-)-cryptowolidine
(+)-(5S)-2-Ethoxycarbonyl-3-methoxy-5-trifluoroacetoamido-6-oxo-3,4,5,6-tetrahydro-1H-cyclohept[c,d]indole
6-(2-Bromo-4,5-dimethoxyphenyl)-2,3,8,9-tetramethoxy-5a-methyl-6,10b-dihydroindeno[1,2-a]inden-5(5aH)-one
10-Desmethoxy-10-N-cystino-dicholchamine
5H-thiazolo[3,2-a]pyrimidine-6-carboxylic acid, 2-[[3-ethoxy-4-hydroxy-5-(2-propenyl)phenyl]methylene]-2,3-dihydro-5-(4-methoxyphenyl)-7-methyl-3-oxo-, ethyl ester, (2E)-
benzo[c]phenanthridin-7(5H)-one, 6,8,9,10-tetrahydro-6-(4-hydroxy-3-methoxyphenyl)-9,9-dimethyl-
2,3,4,7-TETRAMETHOXY-1-O-PRIMEVEROSYLOXYXANTHONE
12-O-METHYLCANDESALVONE_B
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
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