Substructure Search

896

CNc1cc(OC)c(C(=O)[NH+]([O-])C2CN3CCC2CC3)cc1Cl.Cl
Reaction #3859
N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2N)CC1
Reaction #40463
6-chloro-7-(4-methyl-piperazin-1-yl)-8-amino-9H-β-carboline
Yield 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2NC(=O)c2cccnc2Cl)CC1
Reaction #40464
desired compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCC(=O)CC2)c2c(C)c(C)n(-c3ccc(Cl)cc3Cl)c2n1
Reaction #51824
1-(2,4-dichlorophenyl)-4-(4-oxopiperidin-1-yl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridine
Yield 81.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CC=C(C(N)=O)CC2)c2c(C)c(C)n(-c3ccc(Cl)cc3Cl)c2n1
Reaction #51825
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(Cl)cc1NC(=O)N1CCN(Cc2ccccc2)CC1
Reaction #55996
N-(4-amino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63697
Compound 12
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cc(-n2ncc(=O)n(C)c2=O)c(Cl)cc1Cl
Reaction #63698
2-[2,4-dichloro-5-(2-propynyloxy)phenyl]-4-methyl-1,2,4-triazine-3,5(2H,4H)-dione
Yield 81.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2cc(OC(C)C)c(Cl)cc2Cl)c(=O)[nH]c1=O
Reaction #63700
2-[2,4-dichloro-5-(1-methylethoxy)phenyl]-6-methyl-1,2,4-triazine-3,5(2H,4H)-dione
Yield 58.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(-n2ncc(=O)n(CCF)c2=O)c(Cl)cc1Cl
Reaction #63704
2-[2,4-dichloro-5-(1-methylethoxy)phenyl]-4-(2-fluoroethyl)-1,2,4-triazine-3,5(2H,4H)-dione
Yield 36.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)N1CCN(c2ccc(N)cc2Cl)CC1
Reaction #66526
1-(4-(4-amino-2-chlorophenyl)piperazin-1-yl)-2-methylpropan-1-one
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)N1CCN(c2ccc(NC(=O)c3ccccn3)cc2Cl)CC1
Reaction #66527
N-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamide
Yield 18.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1Nc2c(Cl)cc(Cl)c(Cl)c2C2OCCC12
Reaction #75693
Compound 67
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Cl)c(N)c1
Reaction #161204
4-chloro-benzene-1,3-diamine
Yield 110.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)c(Cl)cc1N
Reaction #186033
DOI: 10.1039/C8SC04228D
CC(=O)N(O)C(C)c1cccc(Nc2ccccc2C(=O)NN)c1Cl
Reaction #187204
DOI: 10.1039/C8SC04228D
CCC1CCC(N2CCN(c3ccccc3Cl)CC2)CC1
Reaction #188545
DOI: 10.1039/C8SC04228D
Cn1c(=O)cnn(-c2cc(OS(C)(=O)=O)c(Cl)cc2Cl)c1=O
Reaction #189322
DOI: 10.1039/C8SC04228D
CC(C)C(=O)N1CCN(c2ccc(NC(=O)c3ccccn3)cc2Cl)CC1
Reaction #192247
DOI: 10.1039/C8SC04228D
CCOC(=O)c1nn(-c2ccc(Cl)cc2Cl)c(-c2ccc(Br)[se]2)c1C
Reaction #194110
DOI: 10.1039/C8SC04228D
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