2-phenyl-4-hydroxy-7-methoxy-quinoline

COc1ccc2c(Cl)cc(-c3ccccc3)nc2c1
Reaction #177440
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2c(Cl)cc(-c3ccccc3)nc2c1
Reaction #640619
title compound
수율 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
C=C[C@@H]1C[C@]1(NC(=O)C1CC(Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)C=C1C(=O)OC)C(=O)OC(C)(C)C
Reaction #731015
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)C[C@H]1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #731019
title compound
수율 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
C=CC1CC1(NC(=O)C1CC(Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)CC1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #779712
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCC(NC(=O)C1CC(Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)CC1C(=O)OC)C(=O)OC(C)(C)C
Reaction #1206176
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COc1ccc2c(Cl)cc(-c3ccccc3)nc2c1
Reaction #1313997
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COc1ccc2c(Cl)cc(-c3ccccc3)nc2c1
Reaction #1902875
4-chloro-7-methoxy-2-phenylquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_04
C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)C[C@H]1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #2329605
compound 35
수율 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_03
CCC[C@H](NC(=O)[C@@H]1C[C@@H](Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)C[C@H]1C(=O)OC)C(=O)OC(C)(C)C
Reaction #2329611
43
수율 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_03