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CC(C)n1c(=O)[nH]c2ccccc21

CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCOCC3)CC2)c2ccccc21
Reaction #44859
title compound
Rendimiento 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCOCC3)CC2)c2ccccc21
Reaction #44864
titled compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCOCC3)CC2)c2ccccc21.O=S(=O)(O)c1ccccc1
Reaction #44865
titled compound
Rendimiento 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CCC(=O)OC(C)(C)C)CC2)c2ccccc21
Reaction #44874
title compound
Rendimiento 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCC3)CC2)c2ccccc21
Reaction #44879
titled compound
Rendimiento 216.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(C3(C(=O)O)CCCCC3)CC2)c2ccccc21.Cl
Reaction #44884
1-[4-({[(3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]cyclohexanecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2[nH]c(=O)n(C(C)(C)CCN)c2c1
Reaction #61645
1-(3-amino-1,1-dimethyl-propyl)-6-methyl-1,3-dihydro-benzimidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Cl)ccc2n1C1CCN(CCCNc2ccccc2[N+](=O)[O-])CC1
Reaction #75177
5-chloro-1,3-dihydro-1-{1-[3-(2-nitrophenylamino)propyl]-4-piperidinyl}-2H-benzimidazol-2-one
Rendimiento 78.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccccc1NCCCN1CCC(n2c(=O)[nH]c3cc(Cl)ccc32)CC1
Reaction #75178
1-[1-{3-[N-(2-aminophenyl)amino]propyl}-4-piperidinyl]-5-chloro-1,3-dihydro-2H-benzimidazol-2-one
Rendimiento 70.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N1CCC(N2CCC(n3c(=O)n(CCOC(C)=O)c4ccccc43)CC2)CC1
Reaction #75807
1-[1-(1-methoxycarbonylpiperidin-4-yl)-piperidin-4-yl]-3-(2-acetoxy-ethyl)-1,3-dihydro-2H-benzimidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(N2CCC(n3c(=O)[nH]c4ccccc43)CC2)CC1
Reaction #75814
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)n2c(=O)n(C(C(=O)N3CCC(N4CCN(Cc5ccccc5)CC4)C3)c3ccccc3)c3cc(C#N)ccc32)cc1
Reaction #182256
DOI: 10.1039/C8SC04228D
O=c1[nH]c2ccccc2n1C1CCN(CC#CC(O)c2ccc(F)cc2)CC1
Reaction #191622
DOI: 10.1039/C8SC04228D
O=c1[nH]c2ccccc2n1C1CCN(C2(c3ccccc3)CCCCC2)CC1
Reaction #195723
DOI: 10.1039/C8SC04228D
CCn1c(=O)n(C2CCN(CCCCN3C(=O)c4cc(Cl)ccc4S3(=O)=O)CC2)c2ccc(C)cc21
Reaction #198122
DOI: 10.1039/C8SC04228D
Cn1c(=O)n(C2CCC2)c2ccc(CC(=O)O)cc21
Reaction #205763
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C(c1ccccc1)n1c(=O)[nH]c2ccc(Cl)cc21
Reaction #212026
DOI: 10.1039/C8SC04228D
CC(O)(COc1ccccc1N)CN1CCC(n2c(=O)[nH]c3ccccc32)CC1
Reaction #219760
subtitle compound
Rendimiento 76.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(COc1ccccc1NC(=O)c1ccccn1)CN1CCC(n2c(=O)[nH]c3ccccc32)CC1
Reaction #219761
N-(2-{2-Hydroxy-2-methyl-3-[4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)-1-piperidinyl]propoxy}phenyl)-2-pyridinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1ccccc1OC[C@@H](O)CN1CCC(n2c(=O)[nH]c3cc(F)ccc32)CC1
Reaction #219768
solid
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
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