5-amino-2-methylphenol

—
Reaction #7561
hydrochloride salt
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #7580
hydrochloride salt
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)cc1O
Reaction #44899
4-tert-butyl-N-(3-hydroxy-4-methyl-phenyl)-benzenesulfonamide
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(NCc2ccc(N(C)C)cc2)cc1O
Reaction #76818
5-(4-dimethylamino-benzylamino)-2-methyl-phenol
収率 9.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc(NN)cc1O.Cl
Reaction #88907
title compound
収率 127.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(Nc2ncc(F)c(Nc3ccc(C)c(O)c3)n2)cc1O
Reaction #158542
N2,N4-bis(−3-hydroxy-4-methylphenyl)-5-fluoro-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(Nc2ncc(F)c(Nc3ccc(C)c(O)c3)n2)cc1O
Reaction #163651
N2,N4-bis(-3-hydroxy-4-methylphenyl)-5-fluoro-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNC(=O)c1cc(Oc2cc(N)ccc2C)ccn1
Reaction #165529
3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNC(=O)c1cc(Oc2cc(N)ccc2C)ccn1
Reaction #165546
3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNC(=O)c1cc(Oc2cc(N)ccc2C)ccn1
Reaction #165560
3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)Nc1cccc(C(=O)c2ccc3c(c2)NC(=O)C3=CNc2ccc(C)c(O)c2)c1
Reaction #185148
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(NC(=O)c2cccc(C(C)(C)C#N)c2)cc1O
Reaction #186008
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(Sc2ccc(C(=O)Nc3cccc(N(C)C)c3)cc2Nc2ncnc3ncccc23)cc1
Reaction #211471
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(N(C)c2ccco2)cc1O
Reaction #236538
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(Sc2ccc(C(=O)Nc3cccc(C(F)(F)F)c3)cc2Nc2ncnc3nc(C(C)C)ccc23)cc1
Reaction #241859
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(I)cc1O
Reaction #243036
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(NCc2ccc[nH]2)cc1O
Reaction #243619
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)c1ccc(C(=O)Nc2cccc(C(=O)c3ccc4c(c3)NC(=O)C4=CNc3ccc(C)c(O)c3)c2)s1
Reaction #244617
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2nccc(Nc3ccc(C)c(O)c3)c2cc1OC
Reaction #245429
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(Sc2ccc(C(=O)Nc3ccccc3OC)cc2Nc2ncnc3nc(C(C)C)ccc23)cc1
Reaction #247783
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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