Participa en 113 reacciones

878715

COc1cc2nccc(Oc3ccc(N)cc3F)c2cc1OC
Reaction #43787
product
Rendimiento 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc2nccc(Oc3ccc(NC(=O)c4cccn(-c5ccc(F)cc5)c4=O)cc3F)c2cc1OC
Reaction #43789
product
Rendimiento 36.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc2c(Oc3ccc(NC(=O)c4cccn(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCc1ccccc1
Reaction #43794
product
Rendimiento 64.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCc1nnc(NC(=O)Nc2ccc(Oc3ccnc4cc(OC)c(OC)cc34)c(F)c2)s1
Reaction #180489
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2nccc(Oc3ccc(N)cc3F)c2cc1OC
Reaction #222393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2nccc(Oc3ccc(NC(=O)NC(C)c4nccs4)cc3F)c2cc1OC
Reaction #222650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2nccc(Oc3ccc(NC(=O)NC(C)c4nc(C)cs4)cc3F)c2cc1OC
Reaction #235910
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4ccc(Cl)cc4)cc3F)c2cc1OC
Reaction #268074
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4ccc(-c5ccccc5)cc4)cc3F)c2cc1OC
Reaction #281599
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc2nccc(Oc3ccc(NC(=O)c4c(C)n(CC(C)O)n(-c5ccccc5)c4=O)cc3F)c2cc1OC
Reaction #282661
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4ccccc4)cc3F)c2cc1OC
Reaction #288635
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc2nccc(Oc3ccc(N)cc3F)c2cc1OC
Reaction #375271
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc2nccc(Oc3ccc(NC(=O)c4cc(Br)cn(-c5ccccc5)c4=O)cc3F)c2cc1OC
Reaction #398403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc2nccc(Oc3ccc(NC(=O)c4cc(Br)cn(-c5ccccc5)c4=O)cc3F)c2cc1OC
Reaction #503100
5-bromo-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxamide
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COc1cc2nccc(Oc3cc4sc(N)nc4cc3F)c2cc1OC
Reaction #532627
6-(6,7-dimethoxy-quinolin-4-yloxy)-5-fluoro-benzothiazol-2-ylamine
Rendimiento 48.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1cc2nccc(Oc3cc4sc(N)nc4cc3F)c2cc1OC
Reaction #542982
6-(6,7-dimethoxy-quinolin-4-yloxy)-5-fluoro-benzothiazol-2-ylamine
Rendimiento 48.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1cc2nccc(Oc3cc4sc(N)nc4cc3F)c2cc1OC
Reaction #650149
6-(6,7-dimethoxy-quinolin-4-yloxy)-5-fluoro-benzothiazol-2-ylamine
Rendimiento 48.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCn1cc(C(=O)Nc2ccc(Oc3ccnc4cc(OC)c(OC)cc34)c(F)c2)c(=O)n(-c2ccc(F)cc2)c1=O
Reaction #660594
1-Ethyl-3-(4-fluorophenyl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylicacid [4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl]amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COc1cc2nccc(Oc3ccc(NC(=O)c4cn(C[C@H](O)CO)c(=O)n(-c5ccc(F)cc5)c4=O)cc3F)c2cc1OC
Reaction #660601
1-((S)-2,3-Dihydroxypropyl)-3-(4-fluorophenyl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid [4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CCn1c(=O)c(C(=O)Nc2ccc(Oc3ccnc4cc(OC)c(OC)cc34)c(F)c2)cn(-c2ccc(F)cc2)c1=O
Reaction #660605
3-ethyl-1-(4-fluoro-phenyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid [4-(6,7-dimethoxy-quinolin-4-yloxy)-3-fluoro-phenyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
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