4-propan-2-ylaniline

CC(C)c1ccc(NCc2ccc(N(C)C)cc2)cc1
Reaction #62047
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)c1ccc(NCc2ccc(C(F)(F)F)cc2)cc1
Reaction #62050
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)c1ccc(NCc2ccc(OC(F)F)cc2)cc1
Reaction #62051
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)c1ccc(NCc2ccc(OC(F)(F)F)cc2)cc1
Reaction #62052
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)c1ccc(NC#N)cc1
Reaction #82742
4-isopropylphenyl cyanamide
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)c1ccc(N2CCC(C(=O)O)C2=O)cc1
Reaction #86840
pale green solid
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)c1ccc(Nc2ncc(F)c(Nc3ccc4c(c3)OCCO4)n2)cc1
Reaction #158692
N4-(3,4-ethylenedioxyphenyl)-5-fluoro-N2-(4-isopropylphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)c1ccc(Nc2ncc(F)c(Nc3cccc(O)c3)n2)cc1
Reaction #158697
5-fluoro-N4-(3-hydroxyphenyl)-N2-(4-isopropylphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)c1ccc(Nc2ncc(F)c(Nc3ccc4c(c3)OCCO4)n2)cc1
Reaction #163802
N4-(3,4-ethylenedioxyphenyl)-5-fluoro-N2-(4-isopropylphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)c1ccc(Nc2ncc(F)c(Nc3cccc(O)c3)n2)cc1
Reaction #163807
5-fluoro-N4-(3-hydroxyphenyl)-N2-(4-isopropylphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)c1ccc(NC(=O)C2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #189060
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)c1ccc(NC(=O)c2ccc(Cl)nc2)cc1
Reaction #190235
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)=CC(=O)Nc1ccc(C(C)C)cc1
Reaction #198820
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1ccc(C(C)C)cc1
Reaction #202828
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)c1ccc(NCc2ccc(N(C)C)cc2)cc1
Reaction #221357
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)c1ccc(NCc2ccc(F)cc2)cc1
Reaction #223559
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccccc1Oc1c(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)nc(N2CCOCC2)nc1OCCC(=O)Nc1ccc(C(C)C)cc1
Reaction #226477
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)c1ccc(NC#N)cc1
Reaction #226928
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)c1ccc(NC(=O)C2(NC(=O)OC(C)(C)C)CCN(C(=O)OCc3ccccc3)CC2)cc1
Reaction #233424
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)c1ccc(NCc2ccc3cc(O)c(C(=O)O)cc3c2)cc1
Reaction #263010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Seite 1Weiter