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415990

Nc1ncc(-c2cnn(C3CCNCC3)c2)cc1-c1nc2ncc(F)cc2o1
Reaction #183396
DOI: 10.1039/C8SC04228D
Cc1nc(-c2cc(-c3cnn(C4CCN(C(=O)OC(C)(C)C)CC4)c3)cnc2N)cc2ccccc12
Reaction #185293
DOI: 10.1039/C8SC04228D
CC(Oc1cc(-c2cnn(C3CCNCC3)c2)cnc1N)c1c(Cl)ccc(F)c1Cl
Reaction #194812
DOI: 10.1039/C8SC04228D
Nc1ncc(-c2cnn(C3CCNCC3)c2)cc1N1CCc2c(F)ccc(F)c2C1
Reaction #201877
DOI: 10.1039/C8SC04228D
Cl
Reaction #203403
DOI: 10.1039/C8SC04228D
Nc1ncc(-c2cnn(C3CCNCC3)c2)cc1-c1cc2ccc(F)cc2cn1
Reaction #256670
DOI: 10.1039/C8SC04228D
Nc1ncc(-c2cnn(C3CCNCC3)c2)c2cc(-c3cccc4ccsc34)oc12
Reaction #276716
DOI: 10.1039/C8SC04228D
COc1ccc(-n2nnnc2-c2cc(-c3cnn(C4CCN(C(=O)OC(C)(C)C)CC4)c3)cnc2N)c(F)c1F
Reaction #278950
DOI: 10.1039/C8SC04228D
CC(O)c1nn(C2CCN(C(=O)OC(C)(C)C)CC2)cc1-c1cnc(N)c(-c2nc3ccccc3o2)c1
Reaction #290126
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cnc(N)c(C=O)c3)cn2)CC1
Reaction #328590
tert-butyl 4-[4-(6-amino-5-formylpyridin-3-yl)pyrazol-1-yl]-piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2cnn(C3CCNCC3)c2)cc1-c1nc2ccccc2[nH]1
Reaction #328591
3-(1H-benzimidazol-2-yl)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)pyridin-2-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nnnc2-c2cc(-c3cnn(C4CCNCC4)c3)cnc2N)c(F)c1F
Reaction #369882
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cnc(N)c4oc(Cl)cc34)cn2)CC1
Reaction #395737
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cnc(N)c4oc(Cl)cc34)cn2)CC1
Reaction #476633
title compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cnc(N)c4oc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)cc34)cn2)CC1
Reaction #476670
title compound
Ausbeute 36.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)oc2c(N)ncc(-c3cnn(C4CCN(C(=O)OC(C)(C)C)CC4)c3)c12
Reaction #476671
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cnc(N)c4oc(-c5ccccc5)c(Cl)c34)cn2)CC1
Reaction #476672
tert-butyl 4-[4-(7-amino-3-chloro-2-phenylfuro[2,3-c]pyridin-4-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1ncc(-c2cnn(C3CCNCC3)c2)c2c(Cl)c(-c3ccccc3)oc12
Reaction #476673
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cnc(N)c4oc(-c5cccc6ccsc56)cc34)cn2)CC1
Reaction #476674
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2cnn(C3CCNCC3)c2)c2cc(-c3cccc4ccsc34)oc12
Reaction #476675
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
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