[4-(cyanomethyl)phenyl]-boronic acid

N#CCc1ccc(Oc2ccc3c(c2)S(=O)(=O)NC2CCCN32)cc1
Reaction #58052
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)n1nc(-c2ccc(CC#N)cc2)c2c(N)ncnc21
Reaction #245439
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)NS(=O)(=O)c1ccc(-c2ccc(CC#N)cc2)s1
Reaction #296426
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1noc(-c2ccc(-c3ccc(CC#N)cc3)cc2)c1NC(=O)OC(C)c1ccccc1F
Reaction #300188
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cl.N#CCc1ccc(-c2nccnc2N2CCN(Cc3cnn(-c4ccccc4)c3)CC2)cc1
Reaction #307759
title compound
المردود 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCn1ncc(CN2CCN(c3nccnc3-c3ccc(CC#N)cc3)CC2)c1C.Cl
Reaction #307764
title compound
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1c(CN2CCN(c3nccnc3-c3ccc(CC#N)cc3)CC2)cnn1-c1ccccc1.Cl
Reaction #307787
title compound
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)n1nc(-c2ccc(CC#N)cc2)c2c(N)ncnc21
Reaction #325139
2-(4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenyl)acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)n1nc(-c2ccc(CC#N)cc2)c2c(N)ncnc21
Reaction #325171
2-(4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenyl)acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
N#CCc1ccc(-c2cc(C(N)=O)c3[nH]cc(C4CCS(=O)(=O)CC4)c3c2)cc1
Reaction #402620
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#CCc1ccc(-c2cc(C(N)=O)c3[nH]cc(C4CCS(=O)(=O)CC4)c3c2)cc1
Reaction #474500
5-[4-(Cyanomethyl)phenyl]-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COCCCNC(=O)c1ccc(-n2ncc(-c3ccc(CC#N)cc3)c2O)nc1
Reaction #613721
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CN(CCN1CCN(c2nccnc2-c2ccc(CC#N)cc2)CC1)S(=O)(=O)c1cnn(C)c1.Cl
Reaction #640691
title compound
المردود 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1noc(-c2ccc(-c3ccc(CC#N)cc3)cc2)c1NC(=O)O[C@H](C)c1ccccc1Cl
Reaction #640888
[5-(4′-Cyanomethyl-biphenyl-4-yl)-3-methyl-isoxazol-4-yl]-carbamic acid (R)-1-(2-chloro-phenyl)-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1noc(-c2ccc(-c3ccc(CC#N)cc3)cc2)c1NC(=O)O[C@H](C)c1ccccc1F
Reaction #640889
[5-(4′-Cyanomethyl-biphenyl-4-yl)-3-methyl-isoxazol-4-yl]-carbamic acid (R)-1-(2-fluoro-phenyl)-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1noc(-c2ccc(-c3ccc(CC#N)cc3)cc2)c1NC(=O)O[C@H](C)c1ccccc1F
Reaction #640932
[5-(4′-cyanomethyl-biphenyl-4-yl)-3-methyl-isoxazol-4-yl]-carbamic acid (R)-1-(2-fluoro-phenyl)-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4ccc(CCNC)cc4)cc23)CC1
Reaction #649291
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
COCCCNC(=O)c1ccc(-n2ncc(-c3ccc(CC#N)cc3)c2O)nc1
Reaction #666223
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
N#CCc1ccc(-c2cc(C(N)=O)c3[nH]cc(C4CCS(=O)(=O)CC4)c3c2)cc1
Reaction #743261
5-[4-(Cyanomethyl)phenyl]-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Cl
Reaction #754369
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
الصفحة 1التالي