Ähnlichkeitssuche

18329

NC(=O)[C@H]1CCCC[C@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7122
(1S,2R)-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCC[C@@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7123
cis-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide
Ausbeute 45.1%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7124
(1S,2S)-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCCC[C@@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7125
product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7126
4-[[(1R,2S)-(2-carbamoyl-cyclohexyl)-(4-chlorobenzenesulfonyl)-amino]-methyl]-benzoic acid methyl ester
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(CN([C@@H]2CCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7127
titled compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@H]1N(Cc1ccc(OC(F)(F)F)c(Cl)c1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7128
titled compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@H]1N(Cc1ccc(F)c(Cl)c1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7129
titled compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@H]1N(Cc1ccc(Cl)s1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7130
titled compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@H]1N(Cc1ccc(SC(F)(F)F)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7131
titled compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCC[C@@H]1N(Cc1ccc(OC(F)(F)F)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7132
titled compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCC[C@@H]1N(Cc1ccc(C(F)(F)F)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7133
titled compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCC[C@@H]1N(Cc1ccc(F)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7134
titled compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN([C@H]2CCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7135
titled compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7136
titled compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCC[C@H]1N(Cc1ccc(OC(F)(F)F)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7137
titled compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCC[C@H]1N(Cc1ccc(C(F)(F)F)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7138
titled compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN([C@@H]2CCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7139
titled compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7140
titled compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN([C@H]2CCCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7141
titled compound
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1
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