Busqueda de Subestructura

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Brc1ccc2c(c1)N=C(N1CCN(c3ccccc3)CC1)c1cccc3c1N2CC3
Reaction #4105
product
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)N=C(N1CCN(Cc3ccccc3)CC1)c1cccc3c1N2CC3
Reaction #4106
9-Bromo-6-(4-phenylmethyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(C2=Nc3cc(Br)ccc3N3CCc4cccc2c43)CC1
Reaction #4108
9-Bromo-6-(4-ethoxycarbonyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3c1N2CC3
Reaction #4127
product
Rendimiento 53.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3ccn-2c13
Reaction #4129
product
Rendimiento 42.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4133
product
Rendimiento 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3-n3ccc4cc(Br)cc2c43)CC1
Reaction #4134
product
Rendimiento 75.2%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)N=C(N1CCN(c3ccccc3)CC1)c1cccc3c1N2CC3
Reaction #4163
product
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)N=C(N1CCN(Cc3ccccc3)CC1)c1cccc3c1N2CC3
Reaction #4164
9-Bromo-6-(4-phenylmethyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(C2=Nc3cc(Br)ccc3N3CCc4cccc2c43)CC1
Reaction #4166
9-Bromo-6-(4-ethoxycarbonyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3c1N2CC3
Reaction #4185
product
Rendimiento 53.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3ccn-2c13
Reaction #4187
product
Rendimiento 42.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4191
product
Rendimiento 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3-n3ccc4cc(Br)cc2c43)CC1
Reaction #4192
product
Rendimiento 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCC1OC(=O)N2c3ccc(Br)cc3CC12
Reaction #6331
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCC1OC(=O)N2c3ccc(-c4ccccc4)cc3CC12
Reaction #6332
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H]2CCN(c3ccc(Br)cc3)[C@H]2C1
Reaction #41247
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@H]2CCN(c3ccc(Br)cc3)[C@H]2C1
Reaction #41248
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)c(Br)cc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44441
trans-N-(8-bromo-7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
Rendimiento 130.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(F)c1-c1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCNC2
Reaction #51546
title compound
Rendimiento 5.2%DOI: 10.6084/m9.figshare.5104873.v1
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