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2-[4-[4-[META-(2-METHYLPROPANAMIDO)-PHENYL]-PIPERAZIN-1-YL]-BUTYL]-1,3-DIOXOPERHYDRO-PYRROLO-[1,2-C]-IMIDAZOLE

Compound with spectra: 1 NMR

2-[4-[4-[META-(2-METHYLPROPANAMIDO)-PHENYL]-PIPERAZIN-1-YL]-BUTYL]-1,3-DIOXOPERHYDRO-PYRROLO-[1,2-C]-IMIDAZOLE
SpectraBase Compound ID GuMWy580iSA
InChI InChI=1S/C24H35N5O3/c1-18(2)22(30)25-19-7-5-8-20(17-19)27-15-13-26(14-16-27)10-3-4-11-29-23(31)21-9-6-12-28(21)24(29)32/h5,7-8,17-18,21H,3-4,6,9-16H2,1-2H3,(H,25,30)
InChIKey ISTWNACBFZHHBA-UHFFFAOYSA-N
Mol Weight 441.6 g/mol
Molecular Formula C24H35N5O3
Exact Mass 441.27399 g/mol

View Spectrum of 2-[4-[4-[META-(2-METHYLPROPANAMIDO)-PHENYL]-PIPERAZIN-1-YL]-BUTYL]-1,3-DIOXOPERHYDRO-PYRROLO-[1,2-C]-IMIDAZOLE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
2-[4-[4-(ORTHO-CYANOPHENYL)-PIPERAZIN-1-YL]-BUTYL]-1,3-DIOXOPERHYDRO-PYRROLO-[1,2-C]-IMIDAZOLE
2-[3-[4-(META-AMINOPHENYL)-PIPERAZIN-1-YL]-PROPYL]-1,3-DIOXOPERHYDRO-IMIDAZO-[1,5-A]-PYRIDINE
2-[3-[4-(META-NITROPHENYL)-PIPERAZIN-1-YL]-PROPYL]-1,3-DIOXOPERHYDRO-IMIDAZO-[1,5-A]-PYRIDINE
2-[3-[4-(ORTHO-TOLYL)-PIPERAZIN-1-YL]-PROPYL]-1,3-DIOXOPERHYDRO-IMIDAZO-[1,5-A]-PYRIDINE
2-[3-[4-[META-(2-METHYLPROPANAMIDO)-PHENYL]-PIPERAZIN-1-YL]-PROPYL]-1,4-DIOXOPERHYDRO-PYRROLO-[1,2-A]-PYRAZINE
2-[4-[4-(META-NITROPHENYL)-PIPERAZIN-1-YL]-BUTYL]-1,4-DIOXOPERHYDRO-PYRIDO-[1,2-A]-PYRAZINE
2-[4-[4-(ORTHO-BUTOXYPHENYL)-PIPERAZIN-1-YL]-BUTYL]-1,4-DIOXOPERHYDRO-PYRROLO-[1,2-A]-PYRAZINE
2-[3-[4-(META-(TRIFLUOROMETHYL)-PHENYL)-PIPERAZIN-1-YL]-PROPYL]-1,4-DIOXOPERHYDRO-PYRIDO-[1,2-A]-PYRAZINE
2-[4-[4-(ORTHO-CYANOPHENYL)-PIPERAZIN-1-YL]-BUTYL]-1,4-DIOXOPERHYDRO-PYRIDO-[1,2-A]-PYRAZINE
2-[3-[4-(ORTHO-METHOXYPHENYL)-PIPERAZIN-1-YL]-PROPYL]-1,4-DIOXOPERHYDRO-PYRIDO-[1,2-A]-PYRAZINE
Title Journal or Book Year
Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 5. Study of the Physicochemical Influence of the Pharmacophore on 5-HT1A/α1-Adrenergic Receptor Affinity:  Synthesis of a New Derivative with Mixed 5-HT1A/D2 Antagonist Properties Journal of Medicinal Chemistry 2000
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