4-fluorophenylacetonitrile

Fc1ccc(-c2onc3ccccc23)cc1
Reaction #1243
3-(4-fluorophenyl)-2,1-benzisoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#CC(C(=O)c1cccc(C(F)(F)F)n1)c1ccc(F)cc1
Reaction #8319
2-(4-fluoro-phenyl)-3-oxo-3-(6-trifluoromethyl-pyridin-2-yl)-propionitrile
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #63584
intermediate 13
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COC(=O)C1CC(C#N)(c2ccc(F)cc2)CCC1=O
Reaction #73461
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#CC(C(=O)c1ccncc1)c1ccc(F)cc1
Reaction #83213
2-(4-fluorophenyl)-3-oxo-3-(pyridin-4-yl)propanenitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Fc1ccc(-c2onc3ccc(-c4ccnn4-c4ccccc4F)cc23)cc1
Reaction #88095
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Fc1ccc(-c2onc3ccc(-c4ccnn4-c4ccc(F)cc4)cc23)cc1
Reaction #88102
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Fc1ccc(-c2onc3ccc(-c4ccnn4-c4cccc(F)c4)cc23)cc1
Reaction #88103
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-n2nccc2-c2ccc3noc(-c4ccc(F)cc4)c3c2)cc1
Reaction #88108
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc(-n2nccc2-c2ccc3noc(-c4ccc(F)cc4)c3c2)cc1
Reaction #88114
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Fc1ccc(-c2onc3ccc(-c4ccnn4-c4ccc(Cl)cc4)cc23)cc1
Reaction #88119
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Fc1ccc(-c2onc3ccc(-c4ccnn4-c4ccc(F)cc4F)cc23)cc1
Reaction #88122
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Fc1ccc(-c2onc3ccc(-c4ccnn4-c4ccccn4)cc23)cc1
Reaction #88129
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Fc1ccc(-c2onc3ccc(-c4ccnn4-c4ccccc4Cl)cc23)cc1
Reaction #88131
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#CCc1ccc(N2CCC(=O)CC2)cc1
Reaction #178277
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccccc1C(C#N)c1ccc(F)cc1
Reaction #190107
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC(C(=O)c1cccc(C(F)(F)F)n1)c1ccc(F)cc1
Reaction #212741
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC(C(=O)c1ccnc(Cl)c1)c1ccc(F)cc1
Reaction #223171
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N=C(Cc1ccc(F)cc1)NO
Reaction #229541
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #254624
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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