4-fluoro-2-(trifluromethyl)-benzonitrile

NCc1ccc(F)cc1C(F)(F)F
Reaction #87531
desired product
収率 19.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(O)C(Nc1ccc(C#N)c(C(F)(F)F)c1)C(=O)O
Reaction #185429
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOC1CCCCC1Oc1ccc(C#N)c(C(F)(F)F)c1
Reaction #230934
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1C(C(C)(C)O)CCN1c1ccc(C#N)c(C(F)(F)F)c1
Reaction #234437
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(NCC2CC2)cc1C(F)(F)F
Reaction #254219
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(N2CCC(O)(CCO)CC2)cc1C(F)(F)F
Reaction #276082
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1CN(c2ccc(C#N)c(C(F)(F)F)c2)C(C)CN1
Reaction #276363
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1CN(C(=O)OC(C)(C)C)CCN1c1ccc(C#N)c(C(F)(F)F)c1
Reaction #285396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=CCNc1ccc(C#N)c(C(F)(F)F)c1
Reaction #287106
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)C1N(c2ccc(C#N)c(C(F)(F)F)c2)CCC1(O)C1CC1
Reaction #294707
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)[C@@H](Nc1ccc(C#N)c(C(F)(F)F)c1)C(=O)O
Reaction #325742
title compound
収率 98.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCCCc1nc(-c2ccc(C(F)(F)F)cc2)sc1COc1ccc(C#N)c(C(F)(F)F)c1
Reaction #370499
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#Cc1ccc(Sc2ccc3cc(Br)ccc3c2)cc1C(F)(F)F
Reaction #433859
4-(6-bromonaphth-2-ylthio)-2-trifluoromethylbenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
—
Reaction #500018
solid
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CC1(C)NC(=O)N(c2ccc(C#N)c(C(F)(F)F)c2)C1=O
Reaction #555753
expected compound
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
C[C@H](O)[C@@H](Nc1ccc(C#N)c(C(F)(F)F)c1)C(=O)O
Reaction #557944
final product
収率 55.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
NCc1ccc(F)cc1C(F)(F)F
Reaction #595924
desired product
収率 19.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(C)(C)OC(=O)N1CCC(Nc2ccc(C#N)c(C(F)(F)F)c2)CC1
Reaction #598373
desired compound
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
C[C@H](O)[C@@H](Nc1ccc(C#N)c(C(F)(F)F)c1)C(=O)O
Reaction #650389
final product
収率 55.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
C[C@@H](O)[C@@H](Nc1ccc(C#N)c(C(F)(F)F)c1)C(=O)O
Reaction #650442
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
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