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505848

CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)c(C#N)cc2F)n[nH]1
Reaction #163050
title compound
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)c(C(N)=O)cc2F)n[nH]1
Reaction #163051
title compound
Ausbeute 85.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)c(CN)cc2F)n[nH]1
Reaction #163052
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCc1cc(F)c(Nc2cc(OC(C)C)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163053
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)c(CNS(C)(=O)=O)cc2F)n[nH]1
Reaction #163054
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c(C#N)cc2F)n[nH]1
Reaction #163055
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c(C(N)=O)cc2F)n[nH]1
Reaction #163056
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c(CN)cc2F)n[nH]1
Reaction #163057
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCc1cc(F)c(Nc2cc(OC(C)C)[nH]n2)nc1N[C@@H](C)c1ccc(F)cc1
Reaction #163058
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c(CNS(C)(=O)=O)cc2F)n[nH]1
Reaction #163059
(S)—N-((5-Fluoro-2-(1-(4-fluorophenyl)ethylamino)-6-(5-isopropoxy-1H-pyrazol-3-ylamino)pyridin-3-yl)methyl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(N(Cc2ccc(F)cc2)c2cc(C3CC3)[nH]n2)n1
Reaction #163067
title compound
Ausbeute 2.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c([N+](=O)[O-])cc2F)n[nH]1
Reaction #163070
title compound
Ausbeute 40.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c([N+](=O)[O-])cc2Cl)n[nH]1
Reaction #163071
title compound
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)ccc2[N+](=O)[O-])n[nH]1
Reaction #163072
title compound
Ausbeute 97.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2ccc([N+](=O)[O-])c(N[C@@H](C)c3ccc(F)cc3)n2)n[nH]1
Reaction #163078
title compound
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](CO)c3ccc(F)cc3)ccc2[N+](=O)[O-])n[nH]1
Reaction #163079
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cn3)c(C#N)cc2F)n[nH]1
Reaction #163093
title compound
Ausbeute 58.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(C(C)Nc2nc(Nc3cc(C4CC4)[nH]n3)c(F)cc2C#N)ccc1F
Reaction #163096
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1C#N)c1ccc(F)c(NC(=O)C2CC2)c1
Reaction #163097
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c(C#N)cc2F)n[nH]1
Reaction #163101
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
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