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1172083

CC(O)CN1CCC(Oc2cc(N3CCOCC3)ccc2C(=O)Nc2cc(Cl)ccc2C(=O)Nc2ccc(Cl)cn2)CC1
Reaction #175581
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #211917
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #264786
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #356905
title compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2cc(C(C)(C)C)ccc2C(=O)Nc2cc(Cl)ccc2C(=O)Nc2ccc(Cl)cn2)CC1
Reaction #387773
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #731361
title compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2cc(C(C)(C)C)ccc2C(=O)Nc2cc(Cl)ccc2C(=O)Nc2ccc(Cl)cn2)CC1
Reaction #731365
2-[4-(tert-Butyl)-2-(1-Boc-piperidin-4-yloxy)benzoylamino]-N-(5-chloropyridin-2-yl)-4-chlorobenzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(C(=O)Nc2cc(Cl)ccc2C(=O)Nc2ccc(Cl)cn2)c(OC2CCNCC2)c1.Cl
Reaction #731366
white solid
Ausbeute 46.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCOc1cc(N2CCOCC2)ccc1C(=O)Nc1cc(Cl)ccc1C(=O)Nc1ccc(Cl)cn1
Reaction #731379
2-[2-(2-tert-Butoxycarbonylaminoethoxy)-4-(morpholin-4-yl)-benzoylamino]-4-chloro-N-(5-chloropyridin-2-yl)benzamide
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCOc1cc(N2CCOCC2)ccc1C(=O)Nc1cc(Cl)ccc1C(=O)Nc1ccc(Cl)cn1
Reaction #1038027
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #1075788
title compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2cc(N3CCOCC3)ccc2C(=O)Nc2cc(Cl)ccc2C(=O)Nc2ccc(Cl)cn2)CC1
Reaction #1322110
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #1334219
title compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #1460052
title compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #1460877
title compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #1970119
title compound
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1NC(=O)C1CCNCC1.O=C(O)C(F)(F)F
Reaction #1970218
4-Chloro-N-(5-chloropyridin-2-yl)-2-[(4-piperidinylcarbonyl)amino]benzamide Trifluoroacetate
DOI: 10.6084/m9.figshare.5104873.v1