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1430044

C#CC1(NS(=O)(=O)Cc2ccc(Cl)cc2)CCCCC1
Reaction #192983
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #270272
DOI: 10.1039/C8SC04228D
NS(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #284571
DOI: 10.1039/C8SC04228D
COc1cc(F)c(N2CCN(S(=O)(=O)Cc3ccc(Cl)cc3)CC2)cc1F
Reaction #357130
1-(4-chlorobenzylsulfonyl)-4-(2,5-difluoro-4-methoxyphenyl)piperazine
Ausbeute 100.6%DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O[Si](C)(C)C(C)(C)C)c5c4[C@@]2(CCN3CC2CC2)[C@H]1O5)S(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #517889
target compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O[Si](C)(C)C(C)(C)C)c5c4[C@@]2(CCN3CC2CC2)[C@H]1O5)S(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #654615
target compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2c(C)sc3nc(C)cc(NS(=O)(=O)Cc4ccc(Cl)cc4)c23)c1
Reaction #660879
title compound
Ausbeute 13.2%DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O[Si](C)(C)C(C)(C)C)c5c4[C@@]2(CCN3CC2CC2)[C@H]1O5)S(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #738233
target compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNS(=O)(=O)Cc1ccc(Cl)cc1
Reaction #816436
title compound
Ausbeute 93.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCc2c(CCNS(=O)(=O)Cc3ccc(Cl)c(Cl)c3)n(C(c3ccccc3)c3ccccc3)c3ccc(Cl)cc23)cc1
Reaction #818133
4-(3-{1-Benzhydryl-5-chloro-2-[2-(3,4-dichloro-phenylmethanesulfonylamino)-ethyl]-1H-indol-3-yl}-propyl)-benzoic acid
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #818575
(3,4-dichloro-phenyl)-methanesulfonamide
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCC1=C(c2ccc(Cl)cc2)S(=O)(=O)NC1(C)C
Reaction #834573
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1CCNC(=O)C(NS(=O)(=O)c2ccc(Cl)cc2)C1
Reaction #939162
4-Chloro-N-(5-isopropyl-2-oxo-azepan-3-yl)-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
C#CCCNS(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #941891
solid
Ausbeute 71.2%DOI: 10.6084/m9.figshare.5104873.v1
C[N+](C)(CCNC(=O)c1nc(Cl)c(N)nc1N)CCNS(=O)(=O)Cc1ccc(Cl)cc1.[Br-]
Reaction #970082
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCc1c(CCNS(=O)(=O)Cc2ccc(Cl)c(Cl)c2)n(C(c2ccccc2)c2ccccc2)c2ccc(Cl)cc12)c1ccc(C(=O)O)cc1
Reaction #1076092
desired product
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C#N)C(c2ccc3[nH]nc(NS(=O)(=O)Cc4ccc(Cl)cc4)c3c2)C(C#N)=C(C)N1
Reaction #1125592
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccc(NS(=O)(=O)Cc3ccc(Cl)cc3)cc2)c2ccc3ccccc3c2N1
Reaction #1136998
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(N2CCN(S(=O)(=O)Cc3ccc(Cl)cc3)CC2)cc1F
Reaction #1203744
DOI: 10.1039/C8SC04228D
CC(C#N)(COc1ccc(Cl)cc1)S(=O)(=O)Cc1ccc(Cl)cc1
Reaction #1215452
DOI: 10.1039/C8SC04228D
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