4-bromobenzonitrile

N#Cc1ccc(N2CCC2)cc1
Reaction #527
Ausbeute 62.0%750 AstraZeneca ELN dataset
CCN(CC)c1ccc(C#N)cc1
Reaction #545
Ausbeute 39.2%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)N1CCN(c2ccc(C#N)cc2)CC1
Reaction #726
Ausbeute 82.3%750 AstraZeneca ELN dataset
CC(N)COc1ccc(C#N)cc1
Reaction #1022
desired product
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@H](NC1=NC(=O)C(C)(c2ccc(C#N)cc2)S1)c1ccccc1F
Reaction #74424
4-(2-((S)-1-(2-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #94953
10
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
N#Cc1ccc(NCc2cccc(F)c2)cc1
Reaction #160326
yellow solid
Ausbeute 79.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(Oc2cccc(F)c2)cc1
Reaction #160332
4-((3′-fluoro)phenoxy)benzonitrile
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(Br)c([N+](=O)[O-])c1
Reaction #161247
4-bromo-3-nitrobenzonitrile
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccncc1N1CCN(c2ccc(C#N)cc2)C1=O
Reaction #167245
product
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(C#CCCC(=O)O)cc1
Reaction #188675
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(C)c(N2CCN(c3ccc(C#N)cc3)CC2)c(C)c2c1OC(C)(C)C2
Reaction #192487
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCc1ccc(C#N)cc1
Reaction #218239
4-allylbenzonitrile
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C=CCc1ccc(C#N)cc1
Reaction #219688
4-allylbenzonitrile
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
N#Cc1ccc(Nc2ccccc2C(N)=O)cc1
Reaction #222674
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(N2CCOCC2)cc1
Reaction #229091
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(-c2ccc(F)nc2)cc1
Reaction #229148
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCc1c(OCc2cccc(Nc3ccc(C#N)cc3)c2)ccc(C(C)=O)c1O
Reaction #232436
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(-c2ccc(C=O)cc2)cc1
Reaction #234855
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(C2(O)CCCCC2)cc1
Reaction #239369
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Seite 1Weiter