An 347 Reaktionen beteiligt

12443

Nc1ccc(-c2cc3[nH]c4ccc(O)cc4c3c3c2C(=O)NC3=O)cc1
Reaction #11115
4-(4-Aminophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccc(NC(=O)Nc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)c1
Reaction #45404
desired product
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1c(C(=O)Nc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)cc2ccccc21
Reaction #45439
desired product
Ausbeute 70.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C(=O)Nc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)oc2ccccc12
Reaction #57589
3-methyl-benzofuran-2-carboxylic acid [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amide
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1(C)OB(c2ccc(NC(=O)c3cc4ccccc4o3)cc2)OC1(C)C
Reaction #57590
benzofuran-2-carboxylic acid [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amide
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCN(CC)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #85803
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1ccc(-c2ncn(-c3ccc(C(F)(F)F)cc3)n2)cc1
Reaction #90312
title compound
Ausbeute 74.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)[C@@H](OC(C)(C)C)c1c(C)nc2sc3c(c2c1-c1ccc(N)cc1)CCCC3
Reaction #92245
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CN(C)S(=O)(=O)Nc1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #157764
title compound
Ausbeute 57.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2ccccc2CNC(=O)C(F)(F)F)cc1
Reaction #161274
N-(4′-amino-biphenyl-2-ylmethyl)-2,2,2-trifluoro-acetamide
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2cc(N3CC4CCC(C3)O4)nc(Cl)n2)cc1
Reaction #162593
4-[2-chloro-6-(8-oxa-3-aza-bicyclo[3.2.1]oct-3-yl)-pyrimidin-4-yl]-phenylamine
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2nc(-c3ccccc3)cc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162617
4-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-phenylpyrimidin-2-yl)aniline
Ausbeute 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CS(=O)(=O)Cc1cc(N2CC3CCC(C2)O3)nc(-c2ccc(N)cc2)n1
Reaction #162619
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2nc(N3CC4CCC(C3)O4)cc(C(F)(F)F)n2)cc1
Reaction #162633
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2nc(N3C4CCC3COC4)c(Cl)c(N3C4CCC3COC4)n2)cc1
Reaction #162635
title compound
Ausbeute 61.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C)Cc1cc(N2C3CCC2COC3)nc(-c2ccc(N)cc2)n1
Reaction #162651
4-(4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-((dimethylamino)methyl)pyrimidin-2-yl)aniline
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)N1CCCN(c2ccc(-c3ccc(N)cc3)nn2)CC1
Reaction #168103
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C)CC(=O)Nc1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #175724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(-c2ccc(Cl)nn2)cc1
Reaction #181059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1COCCN1c1cc(C(C)(C)S(=O)(=O)C2CCCCC2)nc(-c2ccc(N)cc2)n1
Reaction #183322
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Seite 1Weiter