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9-METHYL-6,7,10,11-TETRAHYDRO-12-[[8-[(1,2,3,4-TETRAHYDROACRIDIN-9-YL)-AMINO]-HEPTYL]-AMINO]-7,11-METHANOCYCLOOCTA-[B]-QUINOLINE

Compound with spectra: 1 NMR

9-METHYL-6,7,10,11-TETRAHYDRO-12-[[8-[(1,2,3,4-TETRAHYDROACRIDIN-9-YL)-AMINO]-HEPTYL]-AMINO]-7,11-METHANOCYCLOOCTA-[B]-QUINOLINE
SpectraBase Compound ID 3x4fWaa1jhw
InChI InChI=1S/C37H44N4/c1-25-21-26-23-27(22-25)35-34(24-26)41-33-18-10-7-15-30(33)37(35)39-20-12-4-2-3-11-19-38-36-28-13-5-8-16-31(28)40-32-17-9-6-14-29(32)36/h5,7-8,10,13,15-16,18,21,26-27H,2-4,6,9,11-12,14,17,19-20,22-24H2,1H3,(H,38,40)(H,39,41)/t26-,27+/m1/s1
InChIKey DRXDLNAUTXWJSA-SXOMAYOGSA-N
Mol Weight 544.8 g/mol
Molecular Formula C37H44N4
Exact Mass 544.356597 g/mol
Enantiomer InChIKey DRXDLNAUTXWJSA-RRPNLBNLSA-N

View Spectrum of 9-METHYL-6,7,10,11-TETRAHYDRO-12-[[8-[(1,2,3,4-TETRAHYDROACRIDIN-9-YL)-AMINO]-HEPTYL]-AMINO]-7,11-METHANOCYCLOOCTA-[B]-QUINOLINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
N-HEXYL-9-METHYL-3-CHLORO-6,7,10,11-TETRAHYDRO-7,11-ETHANOCYCLOOCTA-[B]-QUINOLIN-12-AMINE
N-HEXYL-9-METHYL-2-NITRO-6,7,10,11-TETRAHYDRO-7,11-ETHANOCYCLOOCTA-[B]-QUINOLIN-12-AMINE
ETHYL-(3-CHLORO-N-HEXYL-6,7,10,11-TETRAHYDRO-7,11-METHANOCYCLOOCTA-[B]-QUINOLIN-9-YL)-ACETATE
2,3-DIFLUORO-N-HEXYL-9-METHYL-6,7,10,11-TETRAHYDRO-7,11-ETHANOCYCLOOCTA-[B]-QUINOLIN-12-AMINE
2,3-Dimethyl-1,5-diphenyl-2,4-diazabicyclo[3.2.0]hept-3-ene-6-carbonitrile
1-Methyl-3-hydroxy-6-de(ethylidene)-18-de(hydroxymethyl)sarpagine
4,12-DICHLORO-N-HEXYL-9-METHYL-6,7,10,11-TETRAHYDRO-7,11-METHANO-CYCLOOCTA-[B]-QUINOLIN-2-AMINE
STYELSAMINE-N(14)-PALMITAMIDE
4-AMINO-5,6,7,8-TETRAHYDRO-2,3-DI-(PARA-METHOXYPHENYL)-FURO-[2,3-B]-QUINOLINE
STYELSAMINE-N(14)-3-METHYLBUT-2-ENAMIDE
Title Journal or Book Year
Palladium-Catalyzed Preparation of N-Alkylated Tacrine and Huprine Compounds European Journal of Organic Chemistry 2010
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