Busqueda de Subestructura

758907

CC(C)(C)OC(=O)N1CCN(c2ccc(Cl)c3cccnc23)CC1
Reaction #845
Rendimiento 24.3%
O=C(O)[C@H]1CN(C(=O)OCc2ccccc2)CCN1c1cc(Cl)c(Cl)cc1[N+](=O)[O-]
Reaction #11904
title compound
Rendimiento 94.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(Cl)cc2)CC1
Reaction #60995
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)O[C@H](CC(=O)N1CCN(c2ccc(Cl)cc2)CC1)c1ccccc1
Reaction #72489
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(Cl)c(Cl)cc2N2CCNC[C@H]12
Reaction #77313
title compound
Rendimiento 113.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(Cl)c(Cl)cc2N2CCNC[C@@H]12
Reaction #77314
title compound
Rendimiento 120.2%DOI: 10.6084/m9.figshare.5104873.v1
OCCCN1CCN(c2ccc(Cl)c(Cl)c2)CC1
Reaction #92496
compound 7p
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCC[C@@H]12
Reaction #156763
title compound
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #156802
title compound
Rendimiento 41.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCCC[C@@H]12
Reaction #156808
title compound
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(=O)Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc21
Reaction #156827
title compound
Rendimiento 9.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(Cc2ccccc2)c2ncc(CN3CCN(c4ccc(Cl)cc4)CC3)cc2N1
Reaction #156833
title compound
Rendimiento 40.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCSCC12
Reaction #156839
title compound
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCOCC12
Reaction #156850
3-((4-(4-chlorophenyl)piperazin-1-yl)methyl)-6a,7,9,10-tetrahydro-[1,4]oxazino[4,3-a]pyrido[3,2-e]pyrazin-6(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CC(=O)Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc21
Reaction #156853
title compound
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN2c3ncc(CN4CCN(c5ccc(Cl)cc5)CC4)cc3NC(=O)C2C1
Reaction #156857
title compound
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCNCC12
Reaction #156858
title compound
Rendimiento 8.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN2c3ncc(CN4CCN(c5ccc(Cl)cc5)CC4)cc3NC(=O)C2C1
Reaction #156859
title compound
Rendimiento 3.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(Cl)cc2[N+](=O)[O-])CC1
Reaction #157030
tert-butyl 4-(4-chloro-2-nitrophenyl)piperazine-1-carboxylate
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(N2CCN(c3nc4c(c(Nc5cccc(CN6CCOCC6)c5)n3)SCC4)CC2)cc1
Reaction #157266
product
Rendimiento 74.5%DOI: 10.6084/m9.figshare.5104873.v1
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