Involved in 70 reactions

COc1ccc(N)c(N)c1

COc1ccc(N)c(NC(=O)c2n[nH]c3ncc(Br)cc23)c1
Reaction #224050
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(N)c(NC(=O)c2cc(C(F)(F)F)nn2C2CCN(CCN(C)C(=O)OC(C)(C)C)CC2)c1
Reaction #240339
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(NC(=O)c2cccc3cc(Oc4ncnc5cc(OC)c(OC)cc45)ccc23)c(N)c1
Reaction #290033
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CNCCCc1nc2ccc(OC)cc2[nH]1
Reaction #307431
[3-(6-Methoxy-1H-benzoimidazol-2-yl)-propyl]-methyl-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1ccc2nc(-c3cccs3)c(=O)[nH]c2c1
Reaction #317400
7-Methoxy-3-thiophen-2-yl-1H-quinoxalin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1ccc2ncc(=O)[nH]c2c1
Reaction #337217
7-methoxyquinoxalin-2(1H)-one
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COc1ccc(NC(=O)CCCCCNC(=O)c2c(C)[nH]c(C=NN=C3C(=O)Nc4ccc(F)cc43)c2C)c(N)c1
Reaction #338852
title compound
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COc1ccc2nc(S)[nH]c2c1
Reaction #360938
titled compound ( 13 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
COc1ccc(NC(=O)c2n[nH]cc2[N+](=O)[O-])c(N)c1
Reaction #393822
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(N)c(NC(=O)c2n[nH]cc2I)c1
Reaction #406933
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc2nc(-c3cccs3)c(=O)[nH]c2c1
Reaction #434886
7-Methoxy-3-thiophen-2-yl-1H-quinoxalin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
Oc1ccc2[nH]c(C3CCNCC3)nc2c1
Reaction #518811
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
COc1ccc2nc(O)c(O)nc2c1
Reaction #551447
2,3-dihydroxy-6-methoxyquinoxaline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_10
COc1ccc2nc(-c3cccs3)c(=O)[nH]c2c1
Reaction #635572
7-Methoxy-3-thiophen-2-yl-1H-quinoxalin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
COC(=O)c1ccc(-c2nc3ccc(OC)cc3[nH]2)cc1
Reaction #666640
title compound
Yield 66.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COc1ccc2[nH]c(CC3CCCCN3C(=O)c3nc(C)sc3-c3ccc(F)cc3)nc2c1
Reaction #685768
title compound
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
O=C1Nc2ccccc2NC2=C1CSC2
Reaction #767333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1ccc(NC(=O)CCCCCNC(=O)C=C2c3ccccc3-c3ccccc32)c(N)c1
Reaction #769638
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1ccc(NS(=O)(=O)c2cc3ccccc3s2)c(NS(=O)(=O)c2cc3ccccc3s2)c1
Reaction #817426
N,N′-(4-methoxy-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
COc1ccc(NC(=O)CCCCCNC(=O)c2c(C)[nH]c(C=NN=C3C(=O)Nc4ccc(F)cc43)c2C)c(N)c1
Reaction #897406
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
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