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Clc1ccc2sccc2n1

N#Cc1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)c1
Reaction #2858
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CCN(Cc2cccc(C#N)c2)C1=O)S(=O)(=O)c1cc2nc(Cl)ccc2s1
Reaction #2859
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(O)c(CN2CC[C@H](NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)c1
Reaction #2861
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N)c(CN2CC[C@H](NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)c1
Reaction #2862
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(CN2CC[C@H](NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)cs1
Reaction #2863
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(CN2CCC(NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)c1
Reaction #209427
DOI: 10.1039/C8SC04228D
COC(=O)c1sc2ccc(OC)nc2c1N
Reaction #233519
DOI: 10.1039/C8SC04228D
Clc1ccc2scc(Br)c2n1
Reaction #313266
title compound
Ausbeute 54.2%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)c1cc(C)nn2c(-c3sc4ccc(Cl)nc4c3Br)c(C)nc12
Reaction #313267
3-(3-bromo-5-chloro-thieno[3,2-b]pyridin-2-yl)-8-(1-ethyl-propyl)-2,6-dimethyl-imidazo[1,2-b]pyridazine
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc2ccc(OC)nc2c1N
Reaction #322250
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc2sccc2nc1-c1ccccc1
Reaction #330752
title compound
Ausbeute 86.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc2ccc(OC)nc2c1N
Reaction #454467
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc2ccc(-c3ccccc3)nc2c1N
Reaction #529961
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc2ccc(-c3cccnc3)nc2c1N
Reaction #529963
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2sc3cccnc3c2n1
Reaction #721725
2-chlorothieno[3,2-b:4,5-b′]dipyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c2sccc2[nH]c1=O
Reaction #789664
DOI: 10.1039/C8SC04228D
CCOC(OCC)C(C)NCc1csc2ccc(Cl)nc12
Reaction #789945
DOI: 10.1039/C8SC04228D
O=Cc1csc2ccc(Cl)nc12
Reaction #806073
title compound
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)[C@H](C)NCc1csc2ccc(Cl)nc12
Reaction #806079
title compound
Ausbeute 30.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)[C@H](C)N(Cc1csc2ccc(Cl)nc12)C(=O)[C@H](Cc1ccc(OC(C)(C)C)cc1)NC(=O)OCC1c2ccccc2-c2ccccc21
Reaction #806084
title compound
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1
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