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52866

C[C@@]1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NC[C@H]3CCC(=O)O3)n21
Reaction #52118
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(-c3cncnc3)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #52119
title compound
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C[C@@]1(Cc2ccc(-c3cncnc3)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NCCC(N)=O)n21
Reaction #52121
title compound
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CC1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCCC3C(N)=O)n21
Reaction #227507
DOI: 10.1039/C8SC04228D
CC(C)(O)CNC(=O)C1CCCN1S(=O)(=O)c1cnc2n1C(C)(Cc1ccc(OC(F)(F)F)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #229780
DOI: 10.1039/C8SC04228D
CC(C)(O)CNC(=O)C1CCCN1S(=O)(=O)c1cnc2n1C(C)(Cc1ccc(C#N)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #301266
DOI: 10.1039/C8SC04228D
CC(=O)NC(=O)C1CCCN1S(=O)(=O)c1cnc2n1C(C)(Cc1ccc(C#N)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #1022396
DOI: 10.1039/C8SC04228D
CC1(Cc2ccc(OC(F)(F)F)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCCC3C(=O)NCCO)n21
Reaction #1029274
DOI: 10.1039/C8SC04228D
COCCNC(=O)C1CCCN1S(=O)(=O)c1cnc2n1C(C)(Cc1ccc(-c3cncnc3)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #1313004
DOI: 10.1039/C8SC04228D
C[C@@]1(Cc2ccc(OC(F)(F)F)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NCCO)n21
Reaction #2461969
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)CNC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(C#N)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #2461971
title compound
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C[C@@]1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)Nc3ccc(O)cc3)n21
Reaction #2461972
title compound
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C[C@@]1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(N)=O)n21
Reaction #2461973
(S)-1-[(R)-5-(4-Cyano-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-sulfonyl]-pyrrolidine-2-carboxylic acid amide
Ausbeute 245.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(C#N)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #2461974
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NC[C@H]3CCC(=O)O3)n21
Reaction #2461975
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CNC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(C#N)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #2461976
title compound
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C[C@@]1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NCC(N)=O)n21
Reaction #2461977
title compound
Ausbeute 56.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(Cc2ccc(C#N)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NCCO)n21
Reaction #2461978
title compound
Ausbeute 104.5%DOI: 10.6084/m9.figshare.5104873.v1
COCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(-c3cncnc3)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #2461979
title compound
Ausbeute 44.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(Cc2ccc(-c3cncnc3)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NCCC(N)=O)n21
Reaction #2461982
title compound
Ausbeute 10.3%DOI: 10.6084/m9.figshare.5104873.v1