Substructure Search

CN1CCN(c2ccc(N)cc2)CC1

COc1cc(N2CCN(C(C)=O)CC2)c(OC)cc1Nc1ncc(Cl)c(-c2cnc3ccccn23)n1
Reaction #209
Yield 0.0%
CC(C)(C)OC(=O)N1CCN(c2ccc(N)cc2)CC1
Reaction #10878
4-(4-aminophenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester
Yield 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10879
4-(4-isothio-cyanatophenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester
Yield 104.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Nc2ccc(N3CCN(CC4CC4)CC3)cc2)sc1C(=O)c1ccc2c(c1)OCO2
Reaction #10913
{4-Amino-2-[4-(4-cyclopropylmethyl-piperazin-1-yl)-phenylamino]-thiazol-5-yl}-benzo[1,3]dioxol-5-yl-methanone
DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@H]2CCN(c3ccc(N4CCN(c5ccc(C#N)cn5)CC4)cc3)[C@H]2C1
Reaction #41239
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc([N+](=O)[O-])ccc2N2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60502
title compound
Yield 14.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc([N+](=O)[O-])ccc2N2CCNCC2)CC(C)(C)C1
Reaction #60503
title compound
Yield 77.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C2CCC1CN(c1ccc(N3CCN(S(C)(=O)=O)CC3)cc1)C2
Reaction #68982
3-[4-(4-methanesulfonylpiperazin-1-yl)phenyl]-3,8-diazabicyclo[3.2.1]-octane-8-carboxylic acid tert-butyl ester
Yield 97.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N)cc2)CC1
Reaction #71333
title compound
Yield 96.7%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1nn(C)c2c1C(C)(C)Cc1cnc(Nc3ccc(N4CCN(C)CC4)cc3)nc1-2.Cl.Cl.Cl
Reaction #72909
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCN(c2ccc(N)cc2)CC1
Reaction #72918
amine
Yield 89.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N)cc2F)CC1
Reaction #85835
tert-butyl 4-(4-amino-2-fluorophenyl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1N1CCNCC1
Reaction #85836
1-(4-bromo-2-fluorophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N3C(=O)c4ccccc4C3=O)c([N+](=O)[O-])c2)CC1
Reaction #86478
title compound
Yield 43.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N)c([N+](=O)[O-])c2)CC1
Reaction #86479
title compound
Yield 94.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(Nc3ncc(Br)c(N(c4ccccc4)C4CCCCC4)n3)cc2)CC1
Reaction #166296
compound 38
Yield 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
CN1CCN(c2ccc(N)c(OC(F)(F)F)c2)CC1
Reaction #169144
4-(4-methyl-piperazin-1-yl)-2-trifluoromethoxy-phenylamine
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(NC(=N)N)c(OC(F)(F)F)c2)CC1
Reaction #169145
title compound
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc([N+](=O)[O-])c(NCc3cccc(Cl)c3)c2)CC1
Reaction #175631
DOI: 10.1039/C8SC04228D
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