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CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CCCC1
Reaction #207983
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)cc2F)c1)C1CC1
Reaction #385888
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CC1
Reaction #478470
N-((5-(3-chloro-4-cyanophenyl)pyridin-3-yl)(cyclopropyl)methyl)ethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CC1
Reaction #478472
title compound
Ausbeute 84.9%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)cc2OC)c1)C1CC1
Reaction #478475
title compound
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(F)c2)c1)C1CC1
Reaction #478477
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)cc2F)c1)C1CC1
Reaction #478479
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CCCC1
Reaction #478481
title compound
Ausbeute 33.4%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)cc2)c1)C1CC1
Reaction #478487
N-((5-(4-cyanophenyl)pyridin-3-yl)(cyclopropyl)methyl)ethanesulfonamide
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CC1)S(=O)(=O)CC
Reaction #478504
ethanesulfonic acid {[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-cyclopropyl-methyl}-ethyl-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc3cc(C#N)ccc3c2)c1)C1CC1
Reaction #478518
title compound
Ausbeute 27.1%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CCCC1
Reaction #773172
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)NC(c1cncc(-c2ccc3cc(C#N)ccc3c2)c1)C1CC1
Reaction #781353
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CC1
Reaction #1217986
DOI: 10.1039/C8SC04228D
CCN(C(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CC1)S(=O)(=O)CC
Reaction #1296599
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CC1
Reaction #1308008
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CC1
Reaction #1984954
N-((5-(3-chloro-4-cyanophenyl)pyridin-3-yl)(cyclopropyl)methyl)ethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C1CC1
Reaction #1984956
title compound
Ausbeute 84.9%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)cc2OC)c1)C1CC1
Reaction #1984959
title compound
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(F)c2)c1)C1CC1
Reaction #1984961
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
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