4-carboxy-2-chlorophenylboronic acid

COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)ccc2c1
Reaction #84063
3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccc(-c2cc(F)c3cc(O)ccc3n2)c(Cl)c1
Reaction #84090
3-chloro-4-(4-fluoro-6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)c1cc(COc2ccc(-c3ccc(C(=O)O)cc3Cl)cc2)n(-c2c(Cl)cccc2Cl)n1
Reaction #187690
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(B(O)O)c(Cl)c1
Reaction #539827
title compound
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)ccc2c1
Reaction #716039
3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
O=C(O)c1ccc(-c2cc(F)c3cc(O)ccc3n2)c(Cl)c1
Reaction #716068
3-chloro-4-(4-fluoro-6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
COC(=O)c1ccc(B(O)O)c(Cl)c1
Reaction #767513
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)ccc2c1
Reaction #1497745
3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
O=C(O)c1ccc(-c2cc(F)c3cc(O)ccc3n2)c(Cl)c1
Reaction #1497773
3-chloro-4-(4-fluoro-6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)ccc2c1
Reaction #1559822
3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
O=C(O)c1ccc(-c2cc(F)c3cc(O)ccc3n2)c(Cl)c1
Reaction #1559850
3-chloro-4-(4-fluoro-6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
O=C(O)c1ccc(-c2ncc3cc(O)ccc3n2)c(Cl)c1
Reaction #1559859
3-chloro-4-(6-hydroxyquinazolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)c(C(F)(F)F)nc2c1
Reaction #1559864
product
Выход 68.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
O=C(O)c1ccc(-c2ccc3c(F)c(O)ccc3n2)c(Cl)c1
Reaction #1559884
final product
Выход 15.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)ccc2c1
Reaction #1594518
3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
O=C(O)c1ccc(-c2cc(F)c3cc(O)ccc3n2)c(Cl)c1
Reaction #1594546
3-chloro-4-(4-fluoro-6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
O=C(O)c1ccc(-c2ncc3cc(O)ccc3n2)c(Cl)c1
Reaction #1594555
3-chloro-4-(6-hydroxyquinazolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)c(C(F)(F)F)nc2c1
Reaction #1594560
product
Выход 68.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
O=C(O)c1ccc(-c2ccc3c(F)c(O)ccc3n2)c(Cl)c1
Reaction #1594580
final product
Выход 15.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COc1ccc2nc(-c3ccc(C(=O)O)cc3Cl)ccc2c1
Reaction #1714795
3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
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