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METHYL-3-BENZYL-1,2,3,4,5,6-HEXAHYDROAZEPINO-[4,5-B]-INDOLE-5-CARBOXYLATE

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

METHYL-3-BENZYL-1,2,3,4,5,6-HEXAHYDROAZEPINO-[4,5-B]-INDOLE-5-CARBOXYLATE
SpectraBase Compound ID 1kpVkvH63AJ
InChI InChI=1S/C21H22N2O2/c1-25-21(24)18-14-23(13-15-7-3-2-4-8-15)12-11-17-16-9-5-6-10-19(16)22-20(17)18/h2-10,18,22H,11-14H2,1H3
InChIKey BLROAGZNDOJDHY-UHFFFAOYSA-N
Mol Weight 334.42 g/mol
Molecular Formula C21H22N2O2
Exact Mass 334.168128 g/mol

View Spectrum of METHYL-3-BENZYL-1,2,3,4,5,6-HEXAHYDROAZEPINO-[4,5-B]-INDOLE-5-CARBOXYLATE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-58-1440-24

View Spectrum of METHYL-3-BENZYL-1,2,3,4,5,6-HEXAHYDROAZEPINO-[4,5-B]-INDOLE-5-CARBOXYLATE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-43-3708-0

View Spectrum of METHYL-3-BENZYL-1,2,3,4,5,6-HEXAHYDROAZEPINO-[4,5-B]-INDOLE-5-CARBOXYLATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 3-(Phenylmethyl)-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indole-5-carboxylic acid methyl ester
Methyl 3-(2-Bromobut-2-en-1-yl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5-carboxylate
Methyl 3-(2-Iodobut-2-en-1-yl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5-carboxylate
3-(2-Ethylallyl)-2,4,5,6-tetrahydro-1H-azepin[4,5-b]indole-5-carboxylic acid methyl ester
Azepino[4,5-b]indole-5-carboxylic acid, 1,2,3,4,5,6-hexahydro-3-(3-oxo-1-butenyl)-, methyl ester
N-Benzyl-N-[2-[2-[2-hydroxy-1-(methoxycarbonyl)ethyl]indol-3-yl]ethyl]-N-[2-acetyl-4-(methoxycarbonyl)butenyl]amine
N-(tert-Butoxycarbonyl)-16-(methoxycarbonyl)-D-norcleavamine
1H-Indole-2-acetic acid, 3-[2-(3,4-dihydro-4-oxo-1(2H)-pyridinyl)ethyl]-.alpha.-(2,2-dimethylpropyl)-, methyl ester, (.+-.)-
t-Butyl 2-[2'-(5"-methyl-2"-oxotetrashydrofuranb-3"-yl)-1H-indol-3'-yl]-ethylcarbamate
(1S)-2-Benzyl-1-(2',2'-dimethoxyethyl)-1,2,3,4-tetrahydro-.beta.-carboline
2-[3-[2-(bis(benzyl)amino)ethyl]-1H-indol-2-yl]-2-hydroxy-propionic acid methyl ester
Title Journal or Book Year
Synthesis of vinca alkaloids and related compounds. 63. A new synthetic pathway for preparing alkaloids and related compounds with the aspidosperma skeleton. Total syntheses of (.+-.)-vincadifformine, (.+-.)-tabersonine, and (.+-.)-oxotabersonine The Journal of Organic Chemistry 1993
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