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1163514

O=[N+]([O-])Nc1cc(Br)nc(Br)c1
Reaction #174548
DOI: 10.1039/C8SC04228D
Nc1ccc(S(=O)(=O)Nc2cc(Br)nc(Br)c2)cc1
Reaction #179473
DOI: 10.1039/C8SC04228D
CCOC(=O)N(Cc1ccc(C(F)(F)F)nc1)c1cc(Br)nc(N)c1[N+](=O)[O-]
Reaction #191631
DOI: 10.1039/C8SC04228D
NC(=S)Nc1cc(Br)nc(Br)c1
Reaction #194130
DOI: 10.1039/C8SC04228D
O=C(NC(=S)Nc1cc(Br)nc(Br)c1)c1ccccc1
Reaction #230554
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccccc1)c1cc(Br)nc(Br)c1
Reaction #278702
DOI: 10.1039/C8SC04228D
CCOC(=O)N(Cc1ccccc1)c1cc(Br)nc(Br)c1[N+](=O)[O-]
Reaction #283620
DOI: 10.1039/C8SC04228D
CCOC(=O)N(Cc1cccc(C#N)c1)c1cc(Br)nc(N)c1[N+](=O)[O-]
Reaction #284200
DOI: 10.1039/C8SC04228D
CCOC(=O)N(Cc1ccccc1)c1cc(Br)nc(N)c1[N+](=O)[O-]
Reaction #285073
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(Br)[n+]([O-])c(Br)c1
Reaction #286392
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1c(Cl)cc(Br)nc1Br
Reaction #296866
DOI: 10.1039/C8SC04228D
CNc1cc(NS(=O)(=O)c2ccc(N)cc2)cc(Br)n1
Reaction #301035
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(F)cc1Oc1cc(Br)nc(Br)c1
Reaction #389068
DOI: 10.1039/C8SC04228D
COc1cc(Br)nc(Br)c1
Reaction #394251
DOI: 10.1039/C8SC04228D
Nc1ccc(S(=O)(=O)Nc2cc(Br)nc(Br)c2)cc1
Reaction #465484
4-amino-N-(2,6-dibromo-pyridin-4-yl)-benzenesulfonamide
Ausbeute 86.5%DOI: 10.6084/m9.figshare.5104873.v1
CNc1cc(NS(=O)(=O)c2ccc(N)cc2)cc(Br)n1
Reaction #465487
4-amino-N-(2-bromo-6-methylamino-pyridin-4-yl)-benzenesulfonamide
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #534245
solid
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)Nc1cc(Br)nc(Br)c1)c1ccccc1
Reaction #534246
desired product
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)Nc1cc(Br)nc(Br)c1
Reaction #534247
desired product
Ausbeute 87.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc2cc(Br)nc(Br)c2s1
Reaction #534248
desired product
Ausbeute 20.1%DOI: 10.6084/m9.figshare.5104873.v1
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