4-bromo-2-fluorobenzonitrile

N#Cc1ccc(N2CCCCC2)cc1F
Reaction #206
Ausbeute 49.4%750 AstraZeneca ELN dataset
N#Cc1ccc(Nc2ccccc2Cl)cc1F
Reaction #346
Ausbeute 83.5%750 AstraZeneca ELN dataset
N#Cc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=O)N3)cc1F
Reaction #7103
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(-c2ccc3c(c2)C2(CCCC2)C(=O)N3)cc1F
Reaction #7109
title compound
Ausbeute 36.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(CCc2sc(-c3ccc(C#N)c(F)c3)cc2C)ccc1OCC12OCC(C)(CO1)CO2
Reaction #9761
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(Cc2cc(Br)ccc2C#N)cc1
Reaction #48110
1-Bromo-4-cyano-3-(4-methoxy-benzyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1ccc(-c2ccc(Cl)cc2Cl)cc1F
Reaction #53586
2-fluoro-4-(2,4-dichlorophenyl)benzonitrile
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc(Br)ccc1C#N
Reaction #57509
4-bromo-2-methoxy-benzonitrile
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccc(CCNC(=O)OCc2ccccc2)cc1F
Reaction #76643
N-[2-(4-cyano-3-fluorophenyl)ethyl](phenylmethoxy)carboxamide
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#Cc1ccc(CCCNC(=O)OCc2ccccc2)cc1F
Reaction #76647
N-[3-(4-cyano-3-fluorophenyl)propyl](phenylmethoxy)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1(C)OC(=O)Nc2ccc(-c3ccc(C#N)c(F)c3)cc21
Reaction #79006
title compound
Ausbeute 6.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccncc1N1CCN(c2ccc(C#N)c(F)c2)C1=O
Reaction #167339
2-Fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzonitrile
Ausbeute 32.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(Br)ccc1C#N
Reaction #188785
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(Br)cc1Sc1ccccc1
Reaction #192645
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cncc(-c2cccc3c2c2ccccc2n3-c2ccc(C#N)c(F)c2)c1
Reaction #193796
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=N)c1ccc(Br)cc1F
Reaction #203148
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(Oc2ccc(C#N)c(F)c2)c2c(c1)OC(C)(C)C2
Reaction #243156
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC1(CC)OC(=O)N(C)c2ccc(Nc3ccc(C#N)c(F)c3)cc21
Reaction #258515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#CCc1cc(Br)ccc1C#N
Reaction #267801
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(-c2ccc(C#N)c(F)c2)cc1
Reaction #293758
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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