3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-quinoline

CC1CCCN1C1CC(c2nc3ccc(-c4cnc5ccccc5c4)cc3s2)C1
Reaction #176210
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1cncc(-c2cnc3ccccc3c2)c1
Reaction #470383
white solid
المردود 98.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Brc1ccc(-c2cnc3ccccc3c2)nc1
Reaction #470384
white solid
المردود 107.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Brc1cncc(-c2cnc3ccccc3c2)c1
Reaction #470385
white solid
المردود 98.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Brc1ccc(-c2cnc3ccccc3c2)nc1
Reaction #470386
white solid
المردود 107.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C[C@H](O)C(=O)N1CCN(Cc2nc3c(N4CCOCC4)nc(-c4cnc5ccccc5c4)nc3s2)CC1
Reaction #1452973
106
المردود 35.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
CS(=O)(=O)N1CCN(Cc2nc3c(N4CCOCC4)nc(-c4cnc5ccccc5c4)nc3s2)CC1
Reaction #1452978
112
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
COc1cc2ncc3c(c2cc1-c1cnc2ccccc2c1)n(-c1ccc(C#N)cc1F)c(=O)n3C
Reaction #1554570
3-fluoro-4-(7-methoxy-3-methyl-2-oxo-8-quinolin-3-yl-2,3-dihydroimidazo[4,5-c]quinolin-1-yl)benzonitrile
المردود 54.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
CS(=O)(=O)N1CCN(Cc2nc3c(N4CCOCC4)nc(-c4cnc5ccccc5c4)nc3s2)CC1
Reaction #1779953
112
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
c1ccc2ncc(-c3ccc4cc[nH]c4c3)cc2c1
Reaction #2025160
المردود 76.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
c1ccc2ncc(-c3ccc4cc[nH]c4c3)cc2c1
Reaction #2025184
المردود 82.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
c1ccc2ncc(-c3ccc4cc[nH]c4c3)cc2c1
Reaction #2025208
المردود 18.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
c1ccc2ncc(-c3ccc4cc[nH]c4c3)cc2c1
Reaction #2025232
المردود 69.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
c1ccc2ncc(-c3ccc4cc[nH]c4c3)cc2c1
Reaction #2025256
المردود 98.0%DOI: 10.1039/c5sc04751jPd_CN_Coupling_Informer_Library
C[C@H]1CCCN1[C@H]1C[C@H](c2nc3ccc(-c4cnc5ccccc5c4)cc3s2)C1
Reaction #2134697
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
C[C@H]1CCCN1[C@H]1C[C@H](c2nc3ccc(-c4cnc5ccccc5c4)cc3s2)C1
Reaction #2190851
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_08