An 82 Reaktionen beteiligt

17460

Cc1ccc(O)cc1Br
Reaction #7003
3-bromo-4-methyl phenol
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)Nc1ccc(C)c(Br)c1
Reaction #58097
title compound
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(NC(=O)C(C)C)cc1Br
Reaction #190773
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(N)cc1Br
Reaction #197010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(N)cc1Br
Reaction #274352
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)cc2)cc1Br
Reaction #284809
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(O)cc1Br
Reaction #285803
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(CNc1ccc(C)c(Br)c1)OCC
Reaction #309104
titled compound
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)cc2)cc1Br
Reaction #360471
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Cc1ccc(Nc2ccccc2CC(=O)O)cc1Br
Reaction #364462
2-[(3-bromo-4-methylphenyl)amino]phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1ccc(NC(=O)C2CC2)cc1Br
Reaction #393649
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)c1ccc(-c2cc(N)ccc2C)cc1
Reaction #438474
methyl 5′-amino-2′-methyl-1,1′-biphenyl-4-carboxylate
Ausbeute 51.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
Cc1ccc(NC(C)C)cc1Br
Reaction #452713
(3-Bromo-4-methyl-phenyl)-isopropyl-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1cc(Br)ccc1S(N)(=O)=O
Reaction #467225
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Cc1ccc(N)cc1Br
Reaction #555973
product
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Cc1ccc(O)cc1Br
Reaction #567838
3-bromo-4-methyl phenol
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
Cc1cc(I)c(N)cc1Br
Reaction #610426
5-bromo-2-iodo-4-methylaniline
Ausbeute 83.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(N)cc1Br
Reaction #671465
expected product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
Cc1ccc(O)cc1Br
Reaction #671466
expected product
Ausbeute 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
COc1cc2ncc(C#N)c(Nc3ccc(C)c(Br)c3)c2cc1OC
Reaction #699345
4-(3-bromo-4-methyl-phenylamino)-6,7-dimethoxy-quinoline-3-carbonitrile
Ausbeute 71.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
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