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(E)-[1-(PARA-TOLYL)-3-[(PARA-TOLYL)-AMINO]-4-CYANO-2-OXOPYRROL-5-YLIDENE]-CYANOACETIC-ACID-ETHYLESTER

Compound with spectra: 1 NMR, and 3 MS (GC)

(E)-[1-(PARA-TOLYL)-3-[(PARA-TOLYL)-AMINO]-4-CYANO-2-OXOPYRROL-5-YLIDENE]-CYANOACETIC-ACID-ETHYLESTER
SpectraBase Compound ID CaDotLH7YPq
InChI InChI=1S/C24H20N4O3/c1-4-31-24(30)20(14-26)22-19(13-25)21(27-17-9-5-15(2)6-10-17)23(29)28(22)18-11-7-16(3)8-12-18/h5-12,27H,4H2,1-3H3/b22-20+
InChIKey YWODCITWOUDZIP-LSDHQDQOSA-N
Mol Weight 412.45 g/mol
Molecular Formula C24H20N4O3
Exact Mass 412.153541 g/mol

View Spectrum of (E)-[1-(PARA-TOLYL)-3-[(PARA-TOLYL)-AMINO]-4-CYANO-2-OXOPYRROL-5-YLIDENE]-CYANOACETIC-ACID-ETHYLESTER

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-64-371-5f

View Spectrum of (E)-[1-(PARA-TOLYL)-3-[(PARA-TOLYL)-AMINO]-4-CYANO-2-OXOPYRROL-5-YLIDENE]-CYANOACETIC-ACID-ETHYLESTER

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-64-371-5e

View Spectrum of (E)-[1-(PARA-TOLYL)-3-[(PARA-TOLYL)-AMINO]-4-CYANO-2-OXOPYRROL-5-YLIDENE]-CYANOACETIC-ACID-ETHYLESTER

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-64-371-5

View Spectrum of (E)-[1-(PARA-TOLYL)-3-[(PARA-TOLYL)-AMINO]-4-CYANO-2-OXOPYRROL-5-YLIDENE]-CYANOACETIC-ACID-ETHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • (E)-[1-(p-Tolyl)-3-[(p-tolyl)amino]-4-cyano-2-oxopyrrol-5-ylidene]cyanoacetic acid ethyl ester
  • (E)-[1-(p-Methoxyphenyl)-3-[(p-methoxyphenyl)amino]-4-cyano-2-oxopyrrol-5-ylidene]cyanoacetic acid ethyl ester
(E)-[1-(PHENYL)-3-(PHENYLAMINO)-4-CYANO-2-OXOPYRROL-5-YLIDENE]-CYANOACETIC-ACID-ETHYLESTER
7,7-Dimethyl-2,5-dioxo-1-phenyl-N-(2,2,6,6-tetramethylpiperidin-4-yl)-1,2,5,6,7,8-hexahydroquinoline-3-carboxamide
(6aR,12aR,12bS)-1,2,3,5,6,6a,7,12,12a,12b-Decahydro-11-methyl-7,7-diphenylindolizino[3,4-b]quinoline
N-(6-cyano-5-(4-methoxyphenyl)-2,4-dioxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-7-yl)-3-oxobutanamide
Diethyl 5-acetyl-1,4-dihydro-6-methyl-1-(3',4'-dimethylphenyl)pyridine-2,3-dicarboxylate
1,6-Dihydro-1-(4-metoxyphenyl)-6-oxo-2,3,4-trimethoxycarbonyl-pyridine
1-(2-fluorophenyl)-4-phenyl-4,6,7,8-tetrahydro-3H-quinoline-2,5-dione
10,10-Dimethyl-11-(tert-butyldiphenylsulfinyl)bicyclo[6.3.0]undec-2-en-6-one
3-quinolinecarboxamide, N-(4-butoxyphenyl)-1-(4-chlorophenyl)-1,2,5,6,7,8-hexahydro-7,7-dimethyl-2,5-dioxo-
methyl 6-amino-4-{5-bromo-2-[(4-chlorobenzyl)oxy]phenyl}-5-cyano-2-methyl-4H-pyran-3-carboxylate
Title Journal or Book Year
Regioselective Synthesis of 5-Ylidenepyrrol-2(5H)-ones by Reaction of Transition Metal-Coordinated Bis(imidoyl) Chlorides with Carbon Nucleophiles The Journal of Organic Chemistry 1999
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