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246568

CCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OC)nc1Cl
Reaction #71711
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71739
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Cl)c(C(C)C)[nH]1
Reaction #71743
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OC)nc1Cl
Reaction #71771
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71772
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@@H]2CCN(C(=O)OC(C)(C)C)C[C@@H]2OC)nc1Cl
Reaction #71782
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=S)n3ccnc3)C[C@H]2OC)nc1Cl
Reaction #71796
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OCC(C)C)nc1Cl
Reaction #71959
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71963
title compound
Ausbeute 117.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)CCN(C(=O)OC(C)(C)C)CC1OCC(F)F
Reaction #71966
title compound
Ausbeute 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71979
title compound
Ausbeute 82.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71981
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OCCCF)nc1Cl
Reaction #71987
title compound
Ausbeute 116.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OCC(C)(F)F)nc1Cl
Reaction #71991
title compound
Ausbeute 94.3%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CNCC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1.Cl
Reaction #71995
title compound
Ausbeute 231.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OC(C)C)nc1Cl
Reaction #72017
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/C(=O)N1CC[C@H](NC(=O)c2nc(Cl)c(CC)[nH]2)[C@H](OC)C1
Reaction #72026
Ethyl cis(±)-(2E)-4-(4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-methoxypiperidin-1-yl)-4-oxo-2-butenoate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cccc(C(=O)OC)n3)C[C@H]2OC)nc1Cl
Reaction #72027
title compound
Ausbeute 120.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCNC[C@H]2OC)nc1Cl.Cl
Reaction #72028
title compound
Ausbeute 201.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc4cccc(C(=O)OC)c4o3)C[C@H]2OC)nc1Cl
Reaction #72098
title compound
Ausbeute 101.5%DOI: 10.6084/m9.figshare.5104873.v1
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