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83056

COc1ccc(S(=O)(=O)N2CCc3ccccc32)cc1O
Reaction #2237
desired product
Ausbeute 100.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCc3ccccc32)cc1OCCCOc1ccccc1
Reaction #2239
title compound
Ausbeute 86.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCc3cc(Br)cc(N)c32)cc1
Reaction #46974
compound 18
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCc3cccc(N)c32)cc1
Reaction #46975
compound 19
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCc3cccc(NC(=O)c4ccccc4)c32)cc1
Reaction #46976
20
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCc3cccc(NC(=O)c4ccncc4)c32)cc1
Reaction #46977
compound 26
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Cl)cc1Cl
Reaction #47149
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #47150
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccccc2)cc1
Reaction #47175
product
Ausbeute 114.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(O)ccc1NS(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #55934
pure intermediate
Ausbeute 84.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Br)cc1
Reaction #57807
4-Bromo-N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCCCC2)cc1
Reaction #57808
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCCC2)cc1
Reaction #57809
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCS(=O)(=O)CC2)cc1
Reaction #57810
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)C[C@H](C)O1
Reaction #57811
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCSCC2)cc1
Reaction #57812
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #57813
amine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCC2)cc1
Reaction #57814
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccnc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Br)cc1
Reaction #57815
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3cccnc3)cc2)C[C@H](C)O1
Reaction #57816
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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