#8105083

CCOC(=O)c1cc(-c2cncc(C)c2)ncc1Br
Reaction #185996
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1cc(-c2cncc(C)c2)ccc1-c1cnccn1
Reaction #189764
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cncc(-c2cc(C)c(Br)c(C)c2)c1
Reaction #324808
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cncc(-c2cc(C)c3c(c2)CN(Cc2ccc(Oc4ccccc4)cc2)C3=O)c1
Reaction #372867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cncc(-c2ccc3ncc4c(c3c2)n(-c2cn(C)nc2C)c(=O)n4C)c1
Reaction #532752
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cc1cncc(-c2nc3c(C)c(F)ccc3cc2C=O)c1
Reaction #659314
title compound
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
Cc1cncc(-c2ccc3c(c2)-c2nc(-c4ncnn4C(C)C)sc2CCO3)c1
Reaction #795124
191
المردود 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Cc1cncc(-c2ccc3c(c2)C2(COC(N)=N2)C2(COC2)C2(CCC2)O3)c1
Reaction #960940
6′-(5-methylpyridin-3-yl)trispiro[cyclobutane-1,2′-chromene-4′,4″-[1,3]oxazole-3′,3′″-oxetan]-2″-amine
المردود 75.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Cc1cncc(-c2cc(C(=O)Nc3ccc(OC(F)(F)F)cc3)cnc2N2CC[C@@H](O)C2)c1
Reaction #1011044
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
Cc1cncc(Cc2ccc(-c3ccccc3)nc2)c1
Reaction #1141304
5-((5-Methylpyridin-3-yl)methyl)-2-phenylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
Cc1cncc(-c2cc(C=O)c(C)o2)c1
Reaction #1200045
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1cncc(-c2ccc3c(c2)-c2nc(-c4ncnn4C(C)C)sc2CCO3)c1
Reaction #1223602
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1cncc(-c2ccc3c(c2)-c2nc(-c4ncnn4C(C)C)sc2CCO3)c1
Reaction #1277582
191
المردود 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
Cc1cncc(-c2nc3cc(F)cc(F)c3c(Cl)c2C)c1
Reaction #1518776
4-chloro-5,7-difluoro-3-methyl-2-(5-methylpyridin-3-yl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_01
Cc1cncc(-c2nc3cc(F)cc(F)c3c(Cl)c2C)c1
Reaction #1705872
4-chloro-5,7-difluoro-3-methyl-2-(5-methylpyridin-3-yl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Cc1cncc(-c2ccc3c(c2)CC(=O)N3C)c1
Reaction #1710677
1-methyl-5-(5-methyl-pyridin-3-yl)-1,3-dihydro-indol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Cc1cncc(-c2cnc(-n3ccc(C)n3)c(C(=O)O)c2)c1
Reaction #1763126
title compound ( 5-2 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
Cc1cncc(-c2nc3cc(NC(=O)c4c(C(=O)N5CCC5)cnn4C)ccn3n2)c1
Reaction #1889436
4-(azetidine-1-carbonyl)-2-methyl-2H-pyrazole-3-carboxylic acid [2-(5-methyl-pyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-yl]-amide
المردود 58.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
Cc1cncc(-c2ccc3c(c2)-c2nc(-c4ncnn4C(C)C)sc2CCO3)c1
Reaction #1936301
191
المردود 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
Cc1cncc(-c2cc(C=O)c(C)o2)c1
Reaction #1964345
title compound
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_11
الصفحة 1التالي