3-Hydroxybenzylamine

O=C(NCc1cccc(O)c1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67871
3-[(2-fluoro-4-iodophenyl)amino]-N-(3-hydroxybenzyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NCc1cccc(O)c1)c1ccncc1Nc1ccc(I)cc1F
Reaction #166036
3-[(2-fluoro-4-iodophenyl)amino]-N-(3-hydroxybenzyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)C(F)(F)F
Reaction #188061
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #224653
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCc1cccc(O)c1)c1ccc(C(=O)O)c(Br)c1
Reaction #240033
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(C(=O)NCc2cccc(O)c2)cc1Cl
Reaction #255354
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCOc1ccc(S(=O)(=O)NCc2cccc(O)c2)cc1-c1nn2c(CCC)nc(C)c2c(=O)[nH]1
Reaction #258874
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #267339
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Oc1cccc(CNc2cncc(Br)c2)c1
Reaction #280064
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1sc(C(=O)NCc2cccc(O)c2)cc1C(C)C
Reaction #283623
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NCc1cccc(O)c1)Oc1ccccc1
Reaction #302373
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NCc1cccc(O)c1)c1ccncc1Nc1ccc(I)cc1F
Reaction #306141
3-[(2-fluoro-4-iodophenyl)amino]-N-(3-hydroxybenzyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)NC(=NCc1cccc(O)c1)NC(=O)OC(C)(C)C
Reaction #450877
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
COC(=O)c1ccc(C(=O)NCc2cccc(O)c2)cc1C
Reaction #480206
4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]-2-methylbenzoic acid, methyl ester
Yield 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
O=C(NCc1cccc(O)c1)Oc1ccccc1
Reaction #742300
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
O=C(NCc1cccc(O)c1)c1ccncc1Nc1ccc(I)cc1F
Reaction #886429
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=c1[nH]nc(Cl)c2cc(NCc3cccc(O)c3)ccc12
Reaction #892680
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Oc1cccc(CNc2ncnc3c2ncn3C2CCCCO2)c1
Reaction #925168
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)NCc1cccc(O)c1
Reaction #989843
titled compound
Yield 22.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
COC(=O)c1ccc(C(=O)NCc2cccc(O)c2)cc1Br
Reaction #1020693
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
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