子结构搜索

566701

CN1C[C@H]2CCN(c3ccc(N4CCN(c5ccc(Cl)nn5)CC4)cc3)[C@H]2C1
Reaction #41242
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)c([N+](=O)[O-])cc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44443
trans-N-(7-chloro-8-nitro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
收率 93.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2c(cc1Cl)N1CCC[C@@H](NC(=O)C(F)(F)F)[C@H]1c1ccccc1O2
Reaction #44444
title compound
收率 96.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)c(N(S(=O)(=O)c4ccccc4)S(=O)(=O)c4ccccc4)cc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44445
trans-N-(7-chloro-2,3,4,14b-tetrahydro-8-[bis(phenylsulfonyl)amino]-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
收率 105.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)c(NS(=O)(=O)c4ccccc4)cc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44446
trans-N-(7-chloro-2,3,4,14b-tetrahydro-8-[(phenylsulfonyl)amino]-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
收率 43.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c(Cl)c1
Reaction #51542
title compound
收率 61.9%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1Cl
Reaction #51543
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(Cl)c(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #51544
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)cc1Cl
Reaction #51545
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Cl)ccc1Nc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCSC2
Reaction #51562
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(CNc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #51565
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(CNc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)cc1Cl
Reaction #51567
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N#Cc1ncc(Cl)cc1Nc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCOC2
Reaction #51575
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ncccc1Nc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCSC2.Cl.Cl
Reaction #51576
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc(C(F)(F)F)ccc1Nc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCOC2.Cl.Cl
Reaction #51577
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ncc(C(F)(F)F)cc1Nc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCOC2.Cl.Cl
Reaction #51578
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c(Cl)c1
Reaction #75824
title compound
收率 61.9%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1Cl
Reaction #75825
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(Cl)c(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #75826
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)cc1Cl
Reaction #75827
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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