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770397

CCOC(=O)Cc1nc2ccc(Br)cc2s1
Reaction #10482
6-bromo-benzothiazol-2-yl-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Br)ccc1S
Reaction #10494
2-Amino-4-bromo-benzenethiol
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc2cc(Cl)ccc2s1
Reaction #57722
5-chloro-benzothiazole-2-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1nc(CSc2ccc(Cl)cc2N)cs1
Reaction #157529
title compound
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)CCSc1ccc(Cl)cc1N
Reaction #157534
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)ccc1SCc1cc([N+](=O)[O-])[nH]n1
Reaction #157536
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1cnc(CSc2ccc(Cl)cc2N)c1
Reaction #157541
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)CCSc1ccc(Cl)cc1N
Reaction #157545
solid
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1nnc(CSc2ccc(Cl)cc2N)[nH]1
Reaction #157548
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)ccc1SCCc1cn[nH]c1
Reaction #157552
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c(C)c1CCSc1ccc(Cl)cc1N
Reaction #157554
title compound
Ausbeute 74.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)ccc1SCc1ccccc1
Reaction #157557
title compound
Ausbeute 112.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)ccc1SCc1ccc([N+](=O)[O-])cc1
Reaction #157563
title compound
Ausbeute 93.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)ccc1SCc1ccccc1[N+](=O)[O-]
Reaction #157565
title compound
Ausbeute 101.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)ccc1SCc1ncccn1
Reaction #157567
title compound
Ausbeute 50.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157572
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cc(Cl)ccc1SCCO)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157573
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cc(Cl)ccc1SCc1ccccn1)c1cc2ccccc2o1
Reaction #157579
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cc(Cl)ccc1SCc1cccnc1)c1cc2ccccc2o1
Reaction #157580
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(CSc2ccc(Cl)cc2NS(=O)(=O)c2ccc(F)cc2F)c1
Reaction #157584
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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