4-phenylmethoxyaniline

Cl.Ic1ccc2ncnc(Nc3ccc(OCc4ccccc4)cc3)c2c1
Reaction #6922
title compound
المردود 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Clc1cc2c(Nc3ccc(OCc4ccccc4)cc3)ncnc2cn1
Reaction #6924
(4-Benzyloxyphenyl)-(6-chloro-pyrido[3,4-d]pyrimidin-4-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NNc1ccc(OCc2ccccc2)cc1
Reaction #65986
product
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Brc1ccc2ncnc(Nc3ccc(OCc4ccccc4)cc3)c2c1.Cl
Reaction #79389
product
المردود 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cl.Ic1ccc2ncnc(Nc3ccc(OCc4ccccc4)cc3)c2c1
Reaction #79390
title compound
المردود 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1c(-c2ccccc2)[nH]c2ccc(OCc3ccccc3)cc12
Reaction #95100
5Benzyloxy-3-methyl-2-phenyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCn1c(=O)n(-c2ccc(OCc3ccccc3)cc2)c2ncc(Cl)cc21
Reaction #169785
3-[4-(benzyloxy)phenyl]-6-chloro-1-ethyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one
المردود 247.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1c(C(F)(F)F)ccnc1Nc1ccc(OCc2ccccc2)cc1
Reaction #169847
title compound
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1cc(F)cnc1Nc1ccc(OCc2ccccc2)cc1
Reaction #169853
title compound
المردود 24.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1cc(F)cnc1Nc1ccc(OCc2ccccc2)cc1
Reaction #169856
title compound
المردود 24.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(C(=O)N(Cc2nc3cc(C#N)ccc3n2CC(=O)Nc2ccc(OCc3ccccc3)cc2)c2ccc(OC3CCN(C(=O)OC(C)(C)C)CC3)cc2)cc1
Reaction #176946
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cnc(Nc2ccc(OCc3ccccc3)cc2)c([N+](=O)[O-])c1
Reaction #178998
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #183767
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(Nc2ccc(OCc3ccccc3)cc2)c(C(=O)O)c1
Reaction #186185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1nnc(-c2ccc3ncnc(Nc4ccc(OCc5ccccc5)cc4)c3c2)o1
Reaction #198011
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NNc1ccc(OCc2ccccc2)cc1
Reaction #209970
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nnc(-c2cc3c(Nc4ccc(OCc5ccccc5)cc4)ncnc3cn2)o1
Reaction #233393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1ccccc1Nc1ccc(OCc2ccccc2)cc1
Reaction #252591
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(CN(C(=O)Nc1ccc(OCc2ccccc2)cc1)c1ccc(Oc2ccccc2)cc1)OC
Reaction #266130
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccnc(C(=O)Nc2ccc(OCc3ccccc3)cc2)c1O
Reaction #266164
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي