Busqueda de Subestructura

CCC(C)N1CCN(c2ccc(N)cc2)CC1

CCC(C)N1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10886
1-(4-isothiocyanatophenyl)-4-(sec-butyl)piperazine
Rendimiento 87.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #10887
1-cyclopentyl-4-(4-nitrophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
S=C=Nc1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #10888
4-cyclopentyl-1-(4 isothiocyanatophenyl)piperazine
Rendimiento 93.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)Nc2ccc(N3CCN(C4CCSCC4)CC3)c(C#N)c2)cnn1-c1ccc(Cl)cc1
Reaction #196454
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(N2CCN(C3CCCCC3)CC2)cc1
Reaction #240945
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(C3CCN(C)CC3)CC2)ccc1Nc1ncc2ccc(-c3ccccc3OC)n2n1
Reaction #242147
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(N3CCN(C4CCN(c5nc6c(cc5F)c(=O)c(C(=O)O)cn6C5CC5)C4)CC3)c(F)c2)C(=O)O1
Reaction #261275
DOI: 10.1039/C8SC04228D
Cc1c(C(=O)Nc2ccc(N3CCN(C4CCOCC4)CC3)c(C#N)c2)cnn1-c1cccc(Cl)c1
Reaction #274258
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #277844
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(C3CCNCC3)CC2)ccc1[N+](=O)[O-]
Reaction #288739
DOI: 10.1039/C8SC04228D
CCOc1cc(N2CCN(C3CCN(CCF)CC3)CC2)ccc1N
Reaction #290586
DOI: 10.1039/C8SC04228D
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Reaction #340102
compound #16
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(N2CCN(C3CCN(CCS(C)(=O)=O)CC3)CC2)ccc1N
Reaction #404493
DOI: 10.1039/C8SC04228D
O=C1NC(=O)c2ccc(I)cc2C1=CNc1ccc(N2CCN(C3CCC3)CC2)cc1
Reaction #407165
DOI: 10.1039/C8SC04228D
CCC(C)N1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #440911
1-(4-isothiocyanatophenyl)-4-(sec-butyl)piperazine
Rendimiento 87.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #440912
1-cyclopentyl-4-(4-nitrophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
S=C=Nc1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #440913
4-cyclopentyl-1-(4-isothiocyanatophenyl)piperazine
Rendimiento 93.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCN(C3CCN(C(=O)OC(C)(C)C)CC3)CC2)ccc1[N+](=O)[O-]
Reaction #506575
title compound
Rendimiento 97.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCN(C3CCNCC3)CC2)ccc1[N+](=O)[O-]
Reaction #506576
title compound
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCN(C3CCN(CCS(C)(=O)=O)CC3)CC2)ccc1N
Reaction #506577
title compound
Rendimiento 63.4%DOI: 10.6084/m9.figshare.5104873.v1
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