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1403555

N#CC=Cc1ccc2c(c1)CCCC2NC(=O)CC(NS(=O)(=O)c1ccc(Cl)c(Cl)c1)c1ccc(F)cc1
Reaction #60378
final compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1ccc2c(c1)CCCC2NC(=O)CC(NS(=O)(=O)c1ccc(Cl)c(Cl)c1)c1ccccc1
Reaction #60389
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)NC1CCC(CCN2CCCC2)CC1
Reaction #205280
DOI: 10.1039/C8SC04228D
N#CC=Cc1ccc2c(c1)CCCC2NC(=O)CC(NS(=O)(=O)c1ccc(Cl)c(Cl)c1)c1ccc(F)cc1
Reaction #250874
DOI: 10.1039/C8SC04228D
COc1cccc2c1-c1ccccc1N(S(=O)(=O)c1ccc(Cl)c(Cl)c1)C2CC(=O)NC1CCC(CCN2CCCC2)CC1
Reaction #292284
DOI: 10.1039/C8SC04228D
COC(=O)CC1c2cc(F)ccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #890574
DOI: 10.1039/C8SC04228D
O=C(O)CC1c2cc(F)ccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #1216346
DOI: 10.1039/C8SC04228D
COC(=O)CC1c2ccccc2CCN1S(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #1729297
Methyl 2-(2-(3,4-dichlorophenylsulfonyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-acetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1c2ccccc2CCN1S(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #1729298
2-(2-(3,4-Dichlorophenylsulfonyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1c2cc(F)ccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #1750423
title compound
Ausbeute 44.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1c2cc(F)ccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #1750424
title compound
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(CC1c2cc(F)ccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)NCCc1ccc(C2=NCCN2)cc1
Reaction #1750425
title compound
Ausbeute 251.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)NCCc1ccc(C2=NCCN2)cc1
Reaction #1750426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)N[C@H]1CC[C@H](CCN2CCCC2)CC1
Reaction #1750427
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)N1CCC(Cc2ccc(C3=NCCN3)cc2)CC1
Reaction #1750428
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)N1CCC(Cc2ccc(C3=NCCCN3)cc2)CC1
Reaction #1750429
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)NCCCN1CCN(c2ccncc2)CC1
Reaction #1750430
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)NCCCN1CCC(N2CCCCC2)CC1
Reaction #1750431
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)NCCN1CCN(c2ccccn2)CC1
Reaction #1750432
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1-c1ccccc1N(S(=O)(=O)c1ccc(Cl)c(Cl)c1)C2CC(=O)NCCc1ccc(C2=NCCN2)cc1.Cl
Reaction #1750441
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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