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METHYL-N-(PARA-TOLYLAMINOCARBONYL)-1,2,7,7A-TETRAHYDRO-1A-H-CYCLOPROPA-[B]-QUINOLINE-1A-CARBOXYLATE

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

METHYL-N-(PARA-TOLYLAMINOCARBONYL)-1,2,7,7A-TETRAHYDRO-1A-H-CYCLOPROPA-[B]-QUINOLINE-1A-CARBOXYLATE
SpectraBase Compound ID DmdewGc6qDE
InChI InChI=1S/C20H20N2O3/c1-13-7-9-16(10-8-13)21-19(24)22-17-6-4-3-5-14(17)11-15-12-20(15,22)18(23)25-2/h3-10,15H,11-12H2,1-2H3,(H,21,24)
InChIKey JYELDEZYMSLYRJ-UHFFFAOYSA-N
Mol Weight 336.39 g/mol
Molecular Formula C20H20N2O3
Exact Mass 336.147393 g/mol

View Spectrum of METHYL-N-(PARA-TOLYLAMINOCARBONYL)-1,2,7,7A-TETRAHYDRO-1A-H-CYCLOPROPA-[B]-QUINOLINE-1A-CARBOXYLATE

MS (GC) Spectrum
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Source of Spectrum J-67-2196-20

View Spectrum of METHYL-N-(PARA-TOLYLAMINOCARBONYL)-1,2,7,7A-TETRAHYDRO-1A-H-CYCLOPROPA-[B]-QUINOLINE-1A-CARBOXYLATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
  • Methyl N-(p-Tolylaminocarbonyl)-1,2,7,7a-tetrahydro-1aH-cyclopropa[b]]quinolin-1a-carboxylate
METHYL-N-PHENYLAMINOCARBONYL-1,2,7,7A-TETRAHYDRO-1A-H-CYCLOPROPA-[B]-QUINOLINE-1A-CARBOXYLATE
METHYL-2-PROPYLAMINOCARBONYL-1,2,7,7A-TETRAHYDRO-1A-H-CYCLOPROPA-[B]-QUINOLINE-1A-CARBOXYLATE
Methyl 2-Propylaminocarbonyl)-1,2,7,7a-tetrahydro-1aH-cyclopropa[b]]quinolin-1a-carboxylate
4,4-Imidazolidinedicarboxylic acid, 5-oxo-1,2,3-triphenyl-, diethyl ester
(7S)-7-methyl-6,7-dihydroquinazolino[3,2-a][1,4]benzodiazepine-5,13-dione
QMACPZZZSHLKJM-UHFFFAOYSA-N
3,4-Quinolinedicarboxylic acid, 2-(3,4-dimethoxyphenyl)-, dimethyl ester
4-Benzoyl-1-(4-bromo-phenyl)-5-(4-methoxy-phenyl)-3-(2-oxo-2-phenyl-ethyl)-1,5-dihydro-pyrrol-2-one
2-ETHYL-2,2-ETHYLENEDIOXY-4,5-DIPHENYL-4,5-DICARBOMETHOXY-1,3,2-DIOXAPHOSPHOLANE
N-(2,4-dimethylphenyl)-2-[2-methyl-3-(2-methylphenyl)-4-oxidanylidene-1H-quinazolin-2-yl]ethanamide
Title Journal or Book Year
Synthesis of 1,2,7,7a-Tetrahydro-1aH-cyclopropa[b]quinoline-1a-carboxylic Acid Derivatives, Doubly Constrained ACC Derivatives, by a Remarkable Cyclopropanation Process The Journal of Organic Chemistry 2002
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