(4-amino-phenyl)-acetic acid ethyl ester

CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCC)c4ccccc4c3OCC)C2=O)cc1
Reaction #43994
ethyl[4-(4,9-diethoxy-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)Cc1ccc(N2Cc3c(c(OCC)c4ccccc4c3OCC)C2)cc1
Reaction #43998
product
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)Cc1ccc(N2Cc3c(cc4ccccc4c3OC)C2=O)cc1
Reaction #44000
ethyl[4-(4-methoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate
Ausbeute 54.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)Cc1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1
Reaction #53023
(Z)-3-[1-(4-ethoxycarbonylmethyl-phenylamino)-1-phenyl-me-thylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)Cc1ccc(NC(=O)/C=C/c2cnn(C)c2-c2ccc(F)cc2)cc1
Reaction #58992
ethyl [4-({(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]prop-2-enoyl}amino)phenyl]acetate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)Cc1ccc(Nc2ncc(C#N)c(Nc3ccc(CC(=O)OCC)cc3)n2)cc1
Reaction #158582
N2,N4-bis[4-(ethoxycarbonylmethyl)phenyl]-5-cyano-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cc1ccc(Nc2ncc(C(F)(F)F)c(Nc3ccc(CC(=O)OCC)cc3)n2)cc1
Reaction #158591
N2,N4-bis[4-(ethoxycarbonylmethyl)phenyl]-5-trifluoromethyl-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cc1ccc(Nc2ncc(C#N)c(Nc3ccc(CC(=O)OCC)cc3)n2)cc1
Reaction #163691
N2,N4-bis[4-(ethoxycarbonylmethyl)phenyl]-5-cyano-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cc1ccc(Nc2ncc(C(F)(F)F)c(Nc3ccc(CC(=O)OCC)cc3)n2)cc1
Reaction #163700
N2,N4-bis[4-(ethoxycarbonylmethyl)phenyl]-5-trifluoromethyl-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cc1ccc(NC=O)cc1
Reaction #169471
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cc1ccc(NC(=O)CCc2cnoc2-c2ccc(Cl)cc2)cc1
Reaction #174077
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cc1ccc(NC(=O)C(CC)NS(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #176216
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cc1ccc(NC(=O)C=Cc2cnn(C)c2-c2ccc(F)cc2)cc1
Reaction #189127
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cc1ccc(NC(=O)C=Cc2c(C)noc2-c2ccccc2)cc1
Reaction #202224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(NS(=O)(=O)c1ccc(Br)cc1)C(=S)Nc1ccc(CC(=O)OCC)cc1
Reaction #203238
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cc1ccc(NC(=O)C23CCC(NCC(=O)N4CC(F)CC4C#N)(CC2)CC3)cc1
Reaction #205427
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cc1ccc(N)c(C(=O)C2CCCC2)c1
Reaction #219039
(4-Amino-3-cyclopentanecarbonylphenyl)acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCNc1ccc(CC(=O)OCC)cc1
Reaction #226895
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCC(NS(=O)(=O)c1ccc(Cl)cc1)C(=O)Nc1ccc(CC(=O)OCC)cc1
Reaction #231620
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)Cc1ccc(NC(=O)C(Cc2ccccc2)NS(=O)(=O)c2ccc(Br)cc2)cc1
Reaction #245572
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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