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(1S,12bS)-10-amino-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester

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

(1S,12bS)-10-amino-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester
SpectraBase Compound ID 5UowtWQBAr9
InChI InChI=1S/C17H21N3O2/c1-22-17(21)13-3-2-7-20-8-6-12-11-5-4-10(18)9-14(11)19-15(12)16(13)20/h4-5,9,13,16,19H,2-3,6-8,18H2,1H3/t13-,16-/m0/s1
InChIKey HXZFSJMGHLBFLT-BBRMVZONSA-N
Mol Weight 299.37 g/mol
Molecular Formula C17H21N3O2
Exact Mass 299.163377 g/mol
Enantiomer InChIKey HXZFSJMGHLBFLT-CZUORRHYSA-N

View Spectrum of (1S,12bS)-10-amino-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester

MS (GC) Spectrum
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Source of Spectrum H1-50-248-5

View Spectrum of (1S,12bS)-10-amino-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Methyl 10-aminoindolo[2,3-a]quinolizidine-1-carboxylate
(1S,12bS)-10-bromo-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester
TRANS-EPIMER
CIS-EPIMER
METHYL-10-METHOXY-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2,3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLATE;CIS-ESTER
METHYL-10-METHOXY-1,2,3,4,6,7,12,12B-ALPHA-OCTAHYDROINDOLO-[2,3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLATE;TRANS-ESTER
1-ALPHA-METHOXYCARBONYL-3-ALPHA-ETHYLINDOLO-[2,3-A]-QUINOLIZIDINE
METHYL-3-ALPHA-ETHYL-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2,3-A]-QUINOLIZINE-1-BETA-CARBOXYLATE
(1S,3S,12bR)-3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-carboxylic acid methyl ester
1-ALPHA-METHOXYCARBONYL-3-BETA-ETHYLINDOLO-[2,3-A]-QUINOLIZIDINE
LTRXZHQPKCCLCI-QSAZIKIQSA-N
Title Journal or Book Year
Substituent Effects on the Rate of Acid-catalysed Epimerization of Indolo[2,3-a]quinolizidines HETEROCYCLES 1999
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