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1429702

C[C@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1cccc(Br)c1
Reaction #43246
desired product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccccc2)c(S(=O)(=O)Nc2ccc(Cl)c(OCCN(C)C)c2)cc1OC
Reaction #51042
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C)cnc1NS(=O)(=O)c1ccccc1Br
Reaction #52040
N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-bromobenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1Br
Reaction #64461
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(S(=O)(=O)c2ccc(C(F)(F)F)cc2Br)CCN1C(=O)OC(C)(C)C
Reaction #71657
title compound
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(S(=O)(=O)c2cc(C(F)(F)F)ccc2Br)CCN1C(=O)OC(C)(C)C
Reaction #71659
crude title compound
Ausbeute 103.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2cc(C(F)(F)F)ccc2Br)CC1
Reaction #71661
1,1-dimethylethyl 4-{[2-bromo-5-(trifluoromethyl)phenyl]sulfonyl}-1-piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)N2CCN(S(=O)(=O)c3ccc(C(F)(F)F)cc3Br)C[C@@H]2C)cn1
Reaction #71664
title compound
Ausbeute 46.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1Br
Reaction #158841
2-bromo-N-t-butyl-benzenesulfonamide
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1Br
Reaction #176596
DOI: 10.1039/C8SC04228D
CC(=O)N1CCc2cc(Br)c(S(=O)(=O)Cl)cc21
Reaction #193207
DOI: 10.1039/C8SC04228D
CC(C)(C)NS(=O)(=O)c1c(Br)cccc1Br
Reaction #205617
DOI: 10.1039/C8SC04228D
CC(C)(C)NS(=O)(=O)c1ccc(C(F)(F)F)cc1Br
Reaction #211770
DOI: 10.1039/C8SC04228D
CC1CN(S(=O)(=O)c2cc(C(F)(F)F)ccc2Br)CCN1C(=O)OC(C)(C)C
Reaction #252710
DOI: 10.1039/C8SC04228D
O=C(NC(CCCCNS(=O)(=O)c1ccccc1Br)C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #265084
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(S(=O)(=O)Nc2ccc3c(c2)B(O)OC3)c(Br)c1)C(F)(F)F
Reaction #281500
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(Br)c(S(=O)(=O)N2CCCCC2)c1
Reaction #293552
DOI: 10.1039/C8SC04228D
Cc1cc(Br)c(S(N)(=O)=O)cc1C(=O)O
Reaction #298551
DOI: 10.1039/C8SC04228D
CC(C)(C)NS(=O)(=O)c1ccccc1Br
Reaction #344436
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1Br
Reaction #344733
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
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