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(Z)-N-(5-Oxo-1,3,4,5-tetrahydrobenz[c,d]indol-4-yl)-2',3'-diethoxycarbonyl-1'-propenylamine

Compound with spectra: 2 NMR, and 1 MS (GC)

(Z)-N-(5-Oxo-1,3,4,5-tetrahydrobenz[c,d]indol-4-yl)-2',3'-diethoxycarbonyl-1'-propenylamine
SpectraBase Compound ID H8uu9nv09xs
InChI InChI=1S/C20H22N2O5/c1-3-26-17(23)9-13(20(25)27-4-2)11-22-16-8-12-10-21-15-7-5-6-14(18(12)15)19(16)24/h5-7,10-11,16,21-22H,3-4,8-9H2,1-2H3/b13-11-
InChIKey DBVDVVDPELJVCB-QBFSEMIESA-N
Mol Weight 370.41 g/mol
Molecular Formula C20H22N2O5
Exact Mass 370.152872 g/mol

View Spectrum of (Z)-N-(5-Oxo-1,3,4,5-tetrahydrobenz[c,d]indol-4-yl)-2',3'-diethoxycarbonyl-1'-propenylamine

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum H1-51-2327-7

View Spectrum of (Z)-N-(5-Oxo-1,3,4,5-tetrahydrobenz[c,d]indol-4-yl)-2',3'-diethoxycarbonyl-1'-propenylamine

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (Z)-N-(5-Oxo-1,3,4,5-tetrahydrobenz[c,d]indol-4-yl)-2',3'-diethoxycarbonyl-1'-propenylamine

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
E-N-(5-OXO-1,3,4,5-TETRAHYDROBENZ-[C,D]-INDOL-4-YL)-2',3'-DIETHOXYCARBONYL-1'-PROPENYLAMINE
RXEHUKXOROKQLF-UHFFFAOYSA-N
N-(5-HYDROXY-1,3,4,5-TETRAHYDROBENZ-[C,D]-INDOL-4-YL)-2',3'-DIETHOXYCARBONYL-1'-PROPENYLAMINE
dl-Clavicipitic acid
(7E)-4-(hydroxymethyl)-7-[(1-methylethyl)imino]-1,4,5,7-tetrahydroazocino[4,5,6-cd]indol-6(3H)-one
(4S,7R)-1,3,4,5,6,7-Hexahydro-7-hydroxy-6-oxopyrrolo[4,3,2-fg][3]benzazocine-4-carboxylic acid methyl ester
7-Azido-1,3,4,5,6,7-hexahydro-4-hydroxymethyl-6-oxopyrrolo[4,3,2-fg][3]benzazocine
CHANOCLAVINE-I
(-)-N(13)-Desmethyl-C12-desisopropyl-C12-phenylmethylindolactam V
(5R, 8R,9S)-5(10-9)-abeo-6-Methyl-8.beta.-hydroxymethyl-ergooline
Title Journal or Book Year
Chemistry of Indoles Carrying a Basic Function. Part IV. Synthesis of D-Nor- ergoline and Ergoline Ring by Stobbe Reaction HETEROCYCLES 1999
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