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780342

N#Cc1cccnc1N1CCC(S(=O)(=O)c2ccc3ccccc3c2)CC1
Reaction #178647
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cccnc1N1CCC(S(=O)(=O)c2cccc(Cl)c2)CC1
Reaction #182299
DOI: 10.1039/C8SC04228D
Cl
Reaction #188134
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(c2cc(C(F)(F)F)ccn2)CC1
Reaction #198332
DOI: 10.1039/C8SC04228D
CC(C)N(CCNC(=O)N1CCCC(S(=O)(=O)c2ccccc2)C1)C(C)C
Reaction #232528
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Cl)cc1)C1CCN(c2c(Cl)cncc2Cl)CC1
Reaction #238949
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(S(=O)(=O)C2CCN(c3ccc4ccccc4n3)CC2)cc1
Reaction #241792
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(S(=O)(=O)C2CCN(c3ncccc3F)CC2)cc1
Reaction #242763
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccccc1)C1CCN(c2ncccc2C(F)(F)F)CC1
Reaction #244251
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2oncc2C(=O)N2CCC(S(=O)(=O)c3ccccc3)C2)cc1
Reaction #264648
DOI: 10.1039/C8SC04228D
CCNCCNC(=O)N1CCCC(S(=O)(=O)c2ccccc2)C1
Reaction #277743
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc2ccccc2c1)C1CCN(c2c(Cl)cncc2Cl)CC1
Reaction #283222
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc2ccccc2c1)C1CCN(c2ncccc2Cl)CC1
Reaction #289561
DOI: 10.1039/C8SC04228D
O=C(O)/C=C\C(=O)O.O=S(=O)(c1ccccc1)C1CCNC1
Reaction #323270
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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
CCN(CC)CCCNC(=O)N1CCC(S(=O)(=O)c2ccccc2)C1.O
Reaction #323293
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CCNC(=O)N1CCCC(S(=O)(=O)c2ccccc2)C1)C(C)C
Reaction #323296
title compound
Rendimiento 59.8%DOI: 10.6084/m9.figshare.5104873.v1
CCNCCNC(=O)N1CCCC(S(=O)(=O)c2ccccc2)C1
Reaction #323298
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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