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CCOC(=O)N1CCC(N)CC1

CC(C)(C)OC(=O)N1CCC(Nc2cccc(-c3ccnc(NCCc4ccc(O)cc4)n3)c2)CC1
Reaction #43012
4-(3-{2-[2-(4-Hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(N(Cc2ccccc2)Cc2ccccc2)C(OC)C1
Reaction #66722
ethyl 4-(dibenzylamino)-3-methoxypiperidine-1-carboxylate
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 #71711
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Br)c(Br)[nH]1
Reaction #71713
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1ncc[nH]1
Reaction #71714
title compound
Ausbeute 58.0%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)[nH]1
Reaction #71720
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnc(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OC)[nH]1
Reaction #71721
title compound
Ausbeute 55.0%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]2OC)nc1C
Reaction #71724
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)nc1Br
Reaction #71729
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Br)c(C)[nH]1
Reaction #71734
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(C(F)(F)F)c[nH]1
Reaction #71738
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
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(C(F)(F)F)c(C)[nH]1
Reaction #71748
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)nc1C(F)(F)F
Reaction #71754
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #71755
title compound
Ausbeute 90.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OC)[nH]c1CC
Reaction #71768
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
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(=O)OC(C)(C)C)C[C@H]2OC)nc1I
Reaction #71784
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(I)c(I)[nH]1
Reaction #71804
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
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