Ähnlichkeitssuche

879482

COC(=O)c1cc2c(Oc3ccc(N)cc3Cl)ccnc2cc1OC
Reaction #199491
DOI: 10.1039/C8SC04228D
CCNC(=O)N1CCC(NC(=O)c2cc3c(Oc4ccc(NC(=S)NC(=O)Cc5ccccc5)cc4F)ccnc3cc2OC)CC1
Reaction #262800
DOI: 10.1039/C8SC04228D
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)Cc4ccccc4)cc3F)c2cc1C(=O)NCCCOC(C)C
Reaction #377118
DOI: 10.1039/C8SC04228D
CCN(CC)CCCOc1cc2c(Oc3ccc(NC(=O)C4(C(=O)Nc5ccc(F)cc5)CC4)cc3F)ccnc2cc1OC
Reaction #532703
N-(4-{[6-{[3-(diethylamino)propyl]oxy}-7-(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)Cc4ccccc4)cc3F)c2cc1C(=O)NCCS(C)(=O)=O
Reaction #775831
DOI: 10.1039/C8SC04228D
CCN(CC)CCCOc1cc2c(Oc3ccc(NC(=O)C4(C(=O)Nc5ccc(F)cc5)CC4)cc3F)ccnc2cc1OC
Reaction #792859
N-(4-{[6-{[3-(diethylamino)propyl]oxy}-7-(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4ccccc4Br)cc3F)c2cc1OC
Reaction #808876
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4ccccc4OC)cc3F)c2cc1OC
Reaction #808878
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4cccc(F)c4)cc3F)c2cc1OC
Reaction #808904
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4ccc(F)cc4)cc3F)c2cc1OC
Reaction #808931
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(=O)NC(=S)Nc2ccc(Oc3ccnc4cc(OC)c(OC)cc34)c(F)c2)cc1
Reaction #808955
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1ccc(C(=O)NC(=S)Nc2ccc(Oc3ccnc4cc(OC)c(OC)cc34)c(F)c2)cc1
Reaction #808956
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4ccc(CCl)cc4)cc3F)c2cc1OC
Reaction #808958
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4ccc(F)cc4F)cc3F)c2cc1OC
Reaction #808971
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)CCc4ccccc4)cc3F)c2cc1OC
Reaction #808986
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)CCC4CCCC4)cc3F)c2cc1OC
Reaction #808987
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)COCc4ccccc4)cc3F)c2cc1OC
Reaction #808990
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)CCCCl)cc3F)c2cc1OC
Reaction #809026
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)CCSC)cc3F)c2cc1OC
Reaction #809027
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)NC(=S)Nc2ccc(Oc3ccnc4cc(OC)c(OC)cc34)c(F)c2)cc1OC
Reaction #809028
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
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