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1156962

FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3ccc4ccccc4n3)cc2)ccc1Cl
Reaction #83337
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(Sc2ccc(NC(=S)Nc3ccc(Cl)c(C(F)(F)F)c3)cc2)nc2ccccc12
Reaction #83339
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3ccc4cc(Cl)ccc4n3)cc2)ccc1Cl
Reaction #83341
title compound
Ausbeute 51.3%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3cc(-c4ccccc4)c4ccccc4n3)cc2)ccc1Cl
Reaction #83343
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(Sc3ccc(NC(=S)Nc4ccc(Cl)c(C(F)(F)F)c4)cc3)ccc2c1
Reaction #83345
title compound
Ausbeute 72.0%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
FC(F)(F)c1ccc2c(Sc3ccc(NC(=S)Nc4ccc(Cl)c(C(F)(F)F)c4)cc3)ccnc2c1
Reaction #83350
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3ccc4ccccc4c3)cc2)ccc1Cl
Reaction #83352
title compound
Ausbeute 34.1%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3nc4ccccc4[nH]3)cc2)ccc1Cl
Reaction #83357
title compound
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3nc4ccccc4o3)cc2)ccc1Cl
Reaction #83359
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3nc4ccccc4s3)cc2)ccc1Cl
Reaction #83361
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3nc4cc(Cl)ccc4s3)cc2)ccc1Cl
Reaction #83363
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Nc3ccc4ccccc4n3)cc2)ccc1Cl
Reaction #83366
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Oc3ccc4ccccc4n3)cc2)ccc1Cl
Reaction #83367
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3ccc4ccccc4c3)cc2)ccc1Cl
Reaction #188901
DOI: 10.1039/C8SC04228D
FC(F)(F)c1cc(N=C=S)ccc1Cl
Reaction #191929
DOI: 10.1039/C8SC04228D
CCC(C)C1CSC(=Nc2ccc(Cl)c(C(F)(F)F)c2)N1
Reaction #293623
DOI: 10.1039/C8SC04228D
FC(F)(F)c1cc(NC(=S)Nc2ccc(Oc3ccc4ccccc4n3)cc2)ccc1Cl
Reaction #299469
DOI: 10.1039/C8SC04228D
CCC(C)[C@H]1CSC(=Nc2ccc(Cl)c(C(F)(F)F)c2)N1
Reaction #363663
(4S)-2-(4-chloro-3-(trifluoromethyl)phenylimino)-4-(2-butyl)-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(-c2nnc(Nc3ccc(Cl)c(C(F)(F)F)c3)o2)cc1
Reaction #474640
title product
Ausbeute 60.8%DOI: 10.6084/m9.figshare.5104873.v1
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