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1362863

Brc1cnc(Nc2ccc(-n3ccnc3)cc2)c2nccn12
Reaction #188215
DOI: 10.1039/C8SC04228D
CN(C)Cc1cn(-c2ccc(Nc3ncc(Br)n4ccnc34)cc2)nn1
Reaction #1031910
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(O)cc1)c1ccc(Nc2ncc(-c3cn[nH]c3)n3ccnc23)cc1
Reaction #1453302
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)c1ccc(Nc2ncc(Br)n3ccnc23)cn1
Reaction #1453308
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cccnc1)c1ccc(Nc2ncc(Br)n3ccnc23)cc1
Reaction #1453310
amide
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc(Nc2ccc(-n3cc(-c4ccccn4)nn3)cc2)c2nccn12
Reaction #1453333
(5-Bromo-imidazo[1,2-a]pyrazin-8-yl)-[4-(4-pyridin-2-yl-[1,2,3]triazol-1-yl)-phenyl]amine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1cn(-c2ccc(Nc3ncc(Br)n4ccnc34)cc2)nn1
Reaction #1453345
title compound
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc(Nc2ccc(-n3ccnc3)cc2)c2nccn12
Reaction #1453347
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnc(-c2ccc(Nc3ncc(Br)n4ccnc34)cc2)n1
Reaction #1453350
title compound
Ausbeute 44.1%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc(Nc2ccc(-n3cc(-c4ccccn4)nn3)cc2)c2nccn12
Reaction #1654843
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(O)cc1)c1ccc(Nc2ncc(-c3cn[nH]c3)n3ccnc23)cc1
Reaction #2008926
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)c1ccc(Nc2ncc(Br)n3ccnc23)cn1
Reaction #2008931
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cccnc1)c1ccc(Nc2ncc(Br)n3ccnc23)cc1
Reaction #2008933
amide
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc(Nc2ccc(-n3cc(-c4ccccn4)nn3)cc2)c2nccn12
Reaction #2008957
(5-Bromo-imidazo[1,2-a]pyrazin-8-yl)-[4-(4-pyridin-2-yl-[1,2,3]triazol-1-yl)-phenyl]-amine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1cn(-c2ccc(Nc3ncc(Br)n4ccnc34)cc2)nn1
Reaction #2008970
title compound
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc(Nc2ccc(-n3ccnc3)cc2)c2nccn12
Reaction #2008972
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnc(-c2ccc(Nc3ncc(Br)n4ccnc34)cc2)n1
Reaction #2008976
title compound
Ausbeute 44.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(O)cc1)c1ccc(Nc2ncc(-c3cn[nH]c3)n3ccnc23)cc1
Reaction #2012076
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)c1ccc(Nc2ncc(Br)n3ccnc23)cn1
Reaction #2012081
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cccnc1)c1ccc(Nc2ncc(Br)n3ccnc23)cc1
Reaction #2012083
amide
DOI: 10.6084/m9.figshare.5104873.v1
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