Busqueda de Subestructura

780388

O=S(=O)(c1ccc(Cl)c(Cl)c1)C1CCN(c2nccc3ccccc23)CC1
Reaction #188627
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Cl)cc1)C1CCN(c2ncccc2Cl)CC1
Reaction #193926
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Cl)cc1)C1CCN(c2c(Cl)cncc2Cl)CC1
Reaction #238949
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(N2CCC(S(=O)(=O)c3ccc(Cl)c(Cl)c3)CC2)CC1
Reaction #265754
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Cl)c(Cl)c1)C1CCN(c2c(Cl)cncc2Cl)CC1
Reaction #287221
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Cl)c(Cl)c1)C1CCN(c2ccc3ccccc3n2)CC1
Reaction #295993
DOI: 10.1039/C8SC04228D
Cl.O=S(=O)(c1ccc(Cl)cc1)C1CCNCC1
Reaction #323277
crystalline solid
Rendimiento 104.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)C2CCNCC2)cc1.Cl
Reaction #323281
4-[(4-Methoxyphenyl)sulfonyl]piperidine monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(S(=O)(=O)c2ccc(Cl)c(Cl)c2)CC1
Reaction #436927
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(N2CCC(S(=O)(=O)c3ccc(Cl)c(Cl)c3)CC2)CC1
Reaction #436928
4-(3,4-dichloro-benzenesulfonyl)-[1,4′]bipiperidinyl-1′-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)N2CCC(N3CCC(S(=O)(=O)c4ccc(Cl)c(Cl)c4)CC3)CC2)cc1
Reaction #436929
[4-(3,4-dichloro-benzenesulfonyl)-[1,4′]bipiperidinyl-1′-yl]-(4-methanesulfonyl-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)c(Cl)c1)C1CCNCC1
Reaction #756356
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Cl)c(Cl)c1)C1CCN(c2ncccc2C(F)(F)F)CC1
Reaction #775785
DOI: 10.1039/C8SC04228D
Cl.O=S(=O)(c1ccc(Cl)cc1)C1(c2cc(F)ccc2F)CCNCC1
Reaction #835984
title compound
Rendimiento 199.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(c2cc(F)ccc2F)(S(=O)(=O)c2ccc(Cl)cc2)CC1
Reaction #835985
title compound
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)cc1)C1(c2cc(F)ccc2F)CCN(Cc2ccccc2)CC1
Reaction #835986
title compound
Rendimiento 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC(c2cc(F)ccc2F)(S(=O)(=O)c2ccc(Cl)cc2)CC1
Reaction #835987
title compound
Rendimiento 54.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC(=O)N1CCC(c2cc(F)ccc2F)(S(=O)(=O)c2ccc(Cl)cc2)CC1
Reaction #835988
title compound
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N1CCC(c2cc(F)ccc2F)(S(=O)(=O)c2ccc(Cl)cc2)CC1
Reaction #835989
title compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccnc1N1CCC(S(=O)(=O)c2ccc(Cl)c(Cl)c2)CC1
Reaction #1029697
DOI: 10.1039/C8SC04228D
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