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COC(=O)C(Cc1ccc2ccccc2c1)N1CCN(S(=O)(=O)c2ccccc2[N+](=O)[O-])C(CCCNC(=O)OCc2ccccc2)C1=O
Reaction #8624
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C(Cc1ccc2ccccc2c1)N1CCNC(CCO[Si](C)(C)C(C)(C)C)C1=O
Reaction #8626
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(N5C(=O)c6ccccc6C5=O)c4)CC3)cccc2n1
Reaction #44116
2-(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(N5Cc6ccccc6C5=O)c4)CC3)cccc2n1
Reaction #44117
title compound
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(NC(=O)c5c(F)cccc5CCl)c4)CC3)cccc2n1
Reaction #44129
2-(chloromethyl)-6-fluoro-N-(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)C(c2cccc(Cl)c2)C2(O)CCCCC2)CC1
Reaction #57080
tert-butyl 4-[(3-chlorophenyl)(1-hydroxycyclohexyl)acetyl]piperazine-1-carboxylate
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(c2cccc(Br)c2)C2(O)CCCCC2)CC1
Reaction #57093
tert-butyl 4-[2-(3-bromophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate
Выход 98.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(c2cccc(-c3ccc(Cl)c(Cl)c3)c2)C2(O)CCCCC2)CC1
Reaction #57094
tert-butyl 4-[2-(3′,4′-dichloro-biphenyl-3-yl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(c2cccc(C#N)c2)C2(O)CCCCC2)CC1
Reaction #57098
tert-butyl 4-[2-(3-cyanophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cccc(C(CN2CCN(C(=O)OC(C)(C)C)CC2)C2(O)CCCCC2)c1
Reaction #57099
tert-butyl 4-[2-(1-hydroxycyclohexyl)-2-(3-vinylphenyl)ethyl]piperazine-1-carboxylate
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.OC1(C(CN2CCNCC2)c2ccc(OCc3ccccc3C(F)(F)F)cc2)CCCCC1
Reaction #57128
1-[2-piperazin-1-yl-1-(4-{[2-(trifluoromethyl)benzyl]oxy}phenyl)ethyl]cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(=O)c2ccc(Cl)cc2Cl)CC1
Reaction #60053
tert-butyl 4-[2-(2,4-dichlorophenyl)-2-oxoethyl]piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C(C(=O)c1ccc(Cl)cc1Cl)N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #60054
tert-butyl 4-{2-(2,4-dichlorophenyl)-1-[(dimethylamino)methylene]-2-oxoethyl}piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(=O)c2ccc(Cl)cc2Cl)CC1
Reaction #60064
tert-butyl 4-[2-(2,4-dichlorophenyl)-2-oxoethyl]piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C(C(=O)c1ccc(Cl)cc1Cl)N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #60065
tert-butyl 4-{2-(2,4-dichlorophenyl)-1-[(dimethylamino)methylene]-2-oxo-ethyl}piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)c1ccccc1)N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #66551
sub-titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(OCC(O)CN3CC4CCCCC3CN4C3CCc4ccccc4C3)cccc2[nH]1
Reaction #68923
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(=O)c2ccc(F)cc2)CC1
Reaction #84623
title compound
Выход 40.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCNCC1)c1ccc(F)cc1
Reaction #84629
title compound
Выход 88.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CCc2ccc(F)cc2F)CC1
Reaction #84633
title compound
Выход 100.3%DOI: 10.6084/m9.figshare.5104873.v1
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