Involved in 109 reactions

1452

COc1ccc(OC)c(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2519
title compound
Yield 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(OC)c(NC(=O)c2cc(Br)ccc2O)c1
Reaction #181943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1cnc(Nc2cc(OC)ccc2OC)[nH]c1=O
Reaction #194492
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(OC)c(Nc2cc(C(F)(F)F)nc(-c3cccnc3)n2)c1
Reaction #203623
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(OC)c(Nc2nc(Cl)nc3ccccc23)c1
Reaction #205088
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(=O)c1cnc2c(C)cccc2c1Nc1cc(OC)ccc1OC
Reaction #212465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(OC)c(Nc2cc(C)nc(-c3ccccn3)n2)c1
Reaction #228775
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CNc1cc(OC)ccc1OC
Reaction #233759
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(OC)c(N2C(=O)c3ccccc3C2=O)c1
Reaction #266105
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(OC)c(NC(=O)Cc2ccccc2)c1
Reaction #291226
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(OC)c(N=C=S)c1
Reaction #318211
2,5-dimethoxyphenylisothiocyanate
Yield 57.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
COc1ccc(OC)c(Nc2cc(C)nc3ccc4nc[nH]c4c23)c1.COc1ccc(OC)c(Nc2cc(C)nc3ccc4nc[nH]c4c23)c1.Cl.Cl.O
Reaction #355441
9-(2,5-Dimethoxyanilino)-7-methyl-1H-imidazo[4,5-f]quinoline Hydrochloride Hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
CCOC(=O)c1c[nH]c2c(OC)ccc(OC)c2c1=O
Reaction #367170
ethyl 1,4-dihydro-5,8-dimethoxy-4-oxo-3-quinolinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
COc1ccc(OC)c(Nc2nc3ccccc3nc2NS(=O)(=O)c2cccc(F)c2)c1
Reaction #418386
title compound
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COc1ccc(OC)c(NC(=O)c2ccccc2OC(C)=O)c1
Reaction #500530
titled compound
Yield 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
COc1ccc(OC)c(NC(=O)c2cc(Br)ccc2O)c1
Reaction #508328
title compound
Yield 39.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COC(=O)c1cccc(Nc2cc(OC)ccc2OC)c1C(=O)OC
Reaction #535536
3-(2,5-Dimethoxyphenylamino)phthalic acid dimethyl ester
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOC(=O)/C(=C\Nc1cc(OC)ccc1OC)c1ccccc1
Reaction #566766
compound 10
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CCOC(=O)/C(=C\Nc1cc(OC)ccc1OC)c1ccc(OC)cc1
Reaction #566772
compound 28
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
COc1ccc(OC)c(NC(=O)c2cc(OC)ccc2OC)c1
Reaction #578885
solid
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
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