4-aminobenzyl alcohol

COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1O
Reaction #8837
combretastatin A-4
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1ccc(NC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
Reaction #42139
title intermediate
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1nc(Cl)cc(Nc2ccc(CO)cc2)n1
Reaction #56841
[4-(2-amino-6-chloro-pyrimidin-4-yl-amino)-phenyl]-methanol
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
OCc1ccc(Nc2nc(Cl)ncc2F)cc1
Reaction #158462
2-chloro-5-fluoro-N4-[4-(hydroxymethyl)phenyl]-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OCc1ccc(Nc2nc(Cl)ncc2F)cc1
Reaction #163573
2-chloro-5-fluoro-N4-[4-(hydroxymethyl)phenyl]-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OCc1ccc(Nc2ncc(C(F)(F)F)c(Cl)n2)cc1
Reaction #188475
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCc1ccc(Nc2ncc(Br)cn2)cc1
Reaction #189388
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1nc(Cl)cc(Nc2ccc(CO)cc2)n1
Reaction #203204
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCc1ccc(N=Cc2nc(-c3ccccc3)cs2)cc1
Reaction #213671
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(CO)cc1)c1ccccn1
Reaction #258225
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(Nc1ccc(CO)cc1)c1ccccn1
Reaction #259301
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N=C(OCc1ccc(N)cc1)C(Cl)(Cl)Cl
Reaction #291685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCc1ccc(Nc2nc(Cl)ncc2F)cc1
Reaction #313737
2-chloro-5-fluoro-N4-[4-(hydroxymethyl)phenyl]-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCCC(=O)c1cnc2c(OC)cccc2c1Nc1ccc(CO)cc1
Reaction #389373
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc(Cl)cc1-c1nc(Cl)nc(Nc2ccc(CO)cc2)n1
Reaction #402336
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=Cc1ccc(NC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
Reaction #405346
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Nc1ccc(CO)cc1)OCc1ccccc1
Reaction #424411
title compound
المردود 57.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COc1ccccc1-n1c(=O)[nH]c2c(C(N)=O)nc(Nc3ccc(Cn4ccnc4)cc3)nc21
Reaction #478844
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(Nc1ccc(CO)cc1)Nc1ccc(-c2nc(N3CCOCC3)nc(N3C4CCC3COC4)n2)cc1
Reaction #491611
title compound
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCCCCCCCCCCCCCOc1ccc(C(=O)Nc2ccc(CO)cc2)cc1
Reaction #570777
desired product
المردود 67.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
الصفحة 1التالي