Busqueda de Subestructura

1172725

O=C(Nc1ccc(N2CCN(Cc3ccccc3)CC2)c(Cl)c1)c1ccccn1
Reaction #66532
N-(4-(4-benzylpiperazin-1-yl)-3-chlorophenyl)picolinamide
Rendimiento 192.2%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cnc(Cl)nc1Nc1ccc(N2CCN(Cc3ccccc3)CC2)cc1
Reaction #158460
N4-[4-(N-benzylpiperazino)phenyl]-2-chloro-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cnc(Nc2ccc(N3CCN(Cc4ccccc4)CC3)cc2)nc1Nc1ccc(N2CCN(Cc3ccccc3)CC2)cc1
Reaction #158594
N2,N4-bis[4-(N-benzylpiperazino)phenyl]-5-fluoro-2,4-pyrimidinediamine
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Nc2ccc3c(c2)OCCO3)ncc1F
Reaction #158660
N2-(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyrimidinediamine
Rendimiento 127.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cnc(Nc2ccc(N3CCN(Cc4ccccc4)CC3)cc2)nc1Nc1ccc2c(c1)OCCO2
Reaction #158662
N2-[4-(N-benzylpiperazino)phenyl]-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyrimidinediamine
Rendimiento 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cnc(Cl)nc1Nc1ccc(N2CCN(Cc3ccccc3)CC2)cc1
Reaction #163571
N4-[4-(N-benzylpiperazino)phenyl]-2-chloro-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cnc(Nc2ccc(N3CCN(Cc4ccccc4)CC3)cc2)nc1Nc1ccc(N2CCN(Cc3ccccc3)CC2)cc1
Reaction #163703
N2,N4-bis[4-(N-benzylpiperazino)phenyl]-5-fluoro-2,4-pyrimidinediamine
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Nc2ccc3c(c2)OCCO3)ncc1F
Reaction #163769
N2-(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyrimidinediamine
Rendimiento 127.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cnc(Nc2ccc(N3CCN(Cc4ccccc4)CC3)cc2)nc1Nc1ccc2c(c1)OCCO2
Reaction #163771
N2-[4-(N-benzylpiperazino)phenyl]-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyrimidinediamine
Rendimiento 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc([N+](=O)[O-])ccc1N1CCN(Cc2ccccc2)CC1COS(C)(=O)=O
Reaction #167691
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC2CN(Cc3ccccc3)CCN2c2ccccc21
Reaction #167692
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1ccccc1)N1CCN(c2ccc(NC(=O)c3cccnc3)cc2)CC1
Reaction #176184
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1)N1CCN(c2ccc([N+](=O)[O-])cc2NCc2ccccc2)CC1
Reaction #177020
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(N2CCN(Cc3ccccc3)CC2)cc1)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #183531
DOI: 10.1039/C8SC04228D
CCC(CC)C(=O)Nc1ccc(N2CCN(C(C(=O)N(CC)CC)c3ccccc3)CC2)c(C#C[Si](C)(C)C)c1
Reaction #183673
DOI: 10.1039/C8SC04228D
Cc1c(C)c2c(c(C)c1O)CCC(C)(C(=O)Nc1ccc(N)cc1)O2
Reaction #186176
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(N2CCNCC2)cc1
Reaction #187434
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc(N2CCN(Cc3ccccc3)CC2)cc1
Reaction #191732
DOI: 10.1039/C8SC04228D
CCC(CC)C(=O)Nc1ccc(N2CCN(C(C(=O)OC)c3ccccc3)CC2)c(F)c1
Reaction #197850
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(N2CCN(Cc3ccccc3)CC2)cc1Nc1ccccc1
Reaction #212284
DOI: 10.1039/C8SC04228D
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