Busqueda de Subestructura

115940

CN1CCN(c2ccc(C(=O)O)nn2)CC1
Reaction #45048
6-(4-methylpiperazin-1-yl)pyridazine-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(C(N)=O)nn2)CC1
Reaction #45049
6-(4-methylpiperazin-1-yl)pyridazine-3-carboxamide
Rendimiento 75.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)C[C@H]2C)nc1
Reaction #70466
title compound
Rendimiento 71.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)C[C@H]2C)cn1
Reaction #70467
title compound
Rendimiento 18.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)C[C@H]2C(=O)OC)nc1C(F)(F)F
Reaction #70469
title compound
Rendimiento 8.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CO)c1cnc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)cn1
Reaction #70474
title compound
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CO)c1ccc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)nc1
Reaction #70475
title compound
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(COS(C)(=O)=O)c1cnc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)cn1
Reaction #70476
title compound
Rendimiento 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC(C)(O)c1cnc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)cn1
Reaction #70477
title compound
Rendimiento 23.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CN1CCC(O)CC1)c1cnc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)cn1
Reaction #70478
title compound
Rendimiento 24.1%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)cc1
Reaction #70479
desired product
Rendimiento 37.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)nc1)N1CCCC1
Reaction #70480
2-{6-[4-(4-Benzyl-phthalazin-1-yl)-piperazin-1-yl]-pyridin-3-yl}-1-pyrrolidin-1-yl-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)c1ccc(N2CCN(c3nnc(Cc4ccc(F)cc4)c4ccccc34)CC2)nc1
Reaction #70486
title compound
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO)C(=O)c1ccc(N2CCN(c3nnc(Cc4ccc(F)cc4)c4ccccc34)CC2)nc1
Reaction #70488
title compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(N2CCN(c3nnc(Cc4ccccc4)c4[nH]cnc34)CC2)nc1
Reaction #70509
title compound
Rendimiento 7.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2ncc(C)n2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(C(F)(F)F)nn2)c1
Reaction #89328
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(C(F)(F)F)nn2)c1
Reaction #89350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(C(F)(F)F)nn2)n1
Reaction #89383
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCN1CCN(c2ccc(-c3ccc(C(F)(F)F)cc3)nn2)CC1.Cl.Cl
Reaction #168062
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(CN2CCN(c3ccc(-c4ccc(C#N)cc4)nn3)CC2)CC1.Cl
Reaction #168065
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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