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70980

—
Reaction #8424
hydrochloride salt
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(S(C)(=O)=O)c(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1C
Reaction #213516
DOI: 10.1039/C8SC04228D
Cc1noc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)c1Br
Reaction #236350
DOI: 10.1039/C8SC04228D
Cc1c(S(=O)(=O)Nc2ccc(Cl)c(N3CCN(C)CC3)c2)sc2ccc(Cl)cc12
Reaction #266708
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)C(F)(F)F)cc1S(=O)(=O)Nc1ccccc1NS(=O)(=O)c1sc2ccc(Cl)cc2c1C
Reaction #295728
DOI: 10.1039/C8SC04228D
Cc1noc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)c1Br
Reaction #319916
N-(4-Bromo-3-methyl-5-isoxazolyl)-5-chloro-3-methylbenzo[b]thiophene-2-sulfonamide
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)c1Br
Reaction #321479
N-(4-bromo-3-methyl-5-isoxazolyl)-5-chloro-3-methylbenzo[b]thiophene-2-sulfonamide
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1sc2ccc(C)cc2c1S(=O)(=O)Cl
Reaction #321571
2-ethyl-5-methylbenzo[b]thiophene-3-sulfonylchloride
DOI: 10.6084/m9.figshare.5104873.v1
CCc1sc2ccc(C)cc2c1S(=O)(=O)Nc1onc(C)c1Br
Reaction #321572
N-(4-bromo-3-methyl-5-isoxazolyl)-2-ethyl-5-methylbenzo[b]thiophene-3-sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(S(=O)(=O)Nc2cccc(C3CN(C(=O)OC(C)(C)C)C3)c2)sc2ccc(Cl)cc12
Reaction #326158
tert-butyl 3-(3-(5-chloro-3-methylbenzo[b]thiophene-2-sulfonamido)phenyl)azetidine-1-carboxylate
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)CNS(=O)(=O)c1sc2ccc(F)cc2c1C
Reaction #373794
DOI: 10.1039/C8SC04228D
Cc1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #380656
DOI: 10.1039/C8SC04228D
Cc1c(S(=O)(=O)NCCO)sc2ccc(Cl)cc12
Reaction #398619
DOI: 10.1039/C8SC04228D
Cc1c(S(=O)(=O)Nc2ccc3[nH]cc(CCN(C)C)c3c2)sc2ccc(Cl)cc12
Reaction #434801
N-[3-(2-dimethylaminoethyl)-1H-indol-5-yl]-5-chloro-3-methyl-benzo[b]thiophene-2-sulphonamide
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2sc(S(=O)(=O)Cl)c(C)c2c1
Reaction #676844
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(S(=O)(=O)Cl)sc2ccc(Br)cc12
Reaction #676846
title compound
Ausbeute 15820.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #676848
title compound
Ausbeute 115.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2sc(S(=O)(=O)Cl)c(C)c2c1
Reaction #676851
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(S(=O)(=O)Cl)sc2ccc(F)cc12
Reaction #676852
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc(NS(=O)(=O)c2sc3ccc(Br)cc3c2C)c1
Reaction #676857
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
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