4-bromoaniline

Clc1ccc2cc(Br)ccc2n1
Reaction #2878
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)=CC(=O)Nc1ccc(Br)cc1
Reaction #6649
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2ccc(Br)cc12
Reaction #9493
1-[3-(6-bromo-3-nitroquinolin-4-ylamino)propyl]pyrrolidin-2-one
Ausbeute 87.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc2sc(Nc3ccc(Br)cc3)nc2c1
Reaction #41720
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2oc(Nc3ccc(Br)cc3)nc2c1
Reaction #41733
(4-bromophenyl)(5-methoxybenzoxazol-2-yl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(Br)cc1C(=O)c1ccc(F)cc1
Reaction #41926
solid
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C#CC(C)(C)Nc1ccc(Br)cc1
Reaction #48313
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=CNc1ccc(Br)cc1
Reaction #51146
N-(4-bromo-phenyl)-formamide
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1=CC(C)(C)Nc2ccc(Br)cc21
Reaction #54095
6-bromo-2,2,4-trimethyl-1,2-dihydroquinoline
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(Cl)cc1-c1cc(Nc2ccc(Br)cc2)nc(N)n1
Reaction #56811
title compound
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Nc1nc(Nc2ccc(Br)cc2)cc(-c2cc(Cl)ccc2Cl)n1
Reaction #56815
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(Cl)cc1-c1cc(Nc2ccc(Br)cc2)nc(N)n1
Reaction #56821
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(Cl)cc1-c1nc(N)cc(Nc2ccc(Br)cc2)n1
Reaction #56831
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1nc(Nc2ccc(Br)cc2)cc(-c2cc(Cl)ccc2C)n1
Reaction #56838
title compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(Br)cc1-c1cc(Nc2ccc(Br)cc2)nc(N)n1
Reaction #56879
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Nc1nc(Nc2ccc(Br)cc2)cc(-c2cc(Br)ccc2OCC(F)(F)F)n1
Reaction #56888
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(Nc1ccc(Br)cc1)c1cc2ccccc2o1
Reaction #57560
N-(4-bromophenyl)-1-benzofuran-2-carboxamide
Ausbeute 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Brc1ccc(N(c2ccccc2)c2ccccc2)cc1
Reaction #60560
diphenylamino 4-bromobenzene
Ausbeute 161.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Brc1ccc(/N=N/N2CCCC2)cc1
Reaction #72704
compound 134
Ausbeute 46.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1ccc(Nc2nnc(Cc3ccncc3)c3ccccc23)cc1
Reaction #78148
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
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