Teilstruktursuche

Sc1ccncc1

NCC(O)C[n+]1ccc(SCC2=C(C(=O)O)N3C(=O)[C@@H](NC(=O)CSc4cc(Cl)ccc4Cl)[C@H]3SC2)cc1.[Cl-]
Reaction #3762
title compound
Ausbeute 127.2%DOI: 10.6084/m9.figshare.5104873.v1
CCSc1ccnc(C2=Cn3c(nc4ccccc43)S2=O)c1C
Reaction #4407
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(C(=O)NCCCSc2ccncc2)cc1.Cl
Reaction #6203
desired compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N(CCCCSc1ccncc1)c1ccccc1N(CCCCSc1ccncc1)C(=O)CC
Reaction #6283
desired product
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N(CCCCSc1ccncc1)c1ccccc1N(CCCCSc1ccncc1)C(=O)CC.Cl.Cl
Reaction #6284
desired product
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)Nc2ccc(Cl)cc2Sc2ccncc2)cc1
Reaction #57917
sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Sc1ccncc1Br
Reaction #74049
ethyl 2-(3-bromopyridin-4-ylthio)-2-methylpropanoate
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Sc1ccncc1-c1ccc(C#N)cc1
Reaction #74050
ethyl 2-(3-(4-cyanophenyl)pyridin-4-ylthio)-2-methylpropanoate
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1cc(-c2ccccc2)c(SCc2ccccc2)c(-c2cccc(C(F)(F)F)c2)c1.[Cl-]
Reaction #74864
4-benzylthio-1-methyl-3-phenyl-5-(3-trifluoromethylphenyl)-pyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccncc2)cc1
Reaction #78724
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3ccnc4ccccc34)cc2)ccc1Cl
Reaction #83347
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc(Nc2ncc(Sc3ccnc(C(=O)NCC(C=O)(c4ccccc4)c4ccccc4)c3F)s2)c1
Reaction #174205
DOI: 10.1039/C8SC04228D
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccncc2)cc1
Reaction #175159
DOI: 10.1039/C8SC04228D
COCCN1CCC(CNC(=O)c2nccc(Sc3cnc(Nc4cc(C)ccn4)s3)c2F)(c2ccncc2)CC1
Reaction #176038
DOI: 10.1039/C8SC04228D
c1ccc(COc2cc(-c3ccccn3)nc(-c3cccc(-c4ccccc4)n3)c2)cc1
Reaction #177246
DOI: 10.1039/C8SC04228D
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccncc2)cc1
Reaction #191775
DOI: 10.1039/C8SC04228D
CSc1c(C#N)c(N)nc(SCc2csc(-c3ccc(Cl)cc3)n2)c1C#N
Reaction #193482
DOI: 10.1039/C8SC04228D
CN(C)CCNc1cc(S(=O)(=O)c2ccc(N)cc2)cc(Br)n1
Reaction #195303
DOI: 10.1039/C8SC04228D
Nc1ccc(S(=O)(=O)c2cc(-c3ccccc3Cl)nc(N3CCCC3)c2)cc1
Reaction #199002
DOI: 10.1039/C8SC04228D
Cc1nc(Nc2ncc(Sc3ccnc(C(=O)O)c3)s2)cc(N2CCN(CCO)CC2)n1
Reaction #201766
DOI: 10.1039/C8SC04228D
Seite 1Weiter