3-chloro-2(1H)-pyridinone hydrazone

CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #90226
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #436563
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #562654
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
—
Reaction #603703
powder
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #603712
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #658850
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #687884
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #729205
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #729784
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
—
Reaction #733821
powder
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #792179
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #896296
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)C1CC(=O)NN1c1ncccc1Cl
Reaction #1260725
title compound
Ausbeute 89.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
—
Reaction #1381738
powder
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
—
Reaction #1435692
powder
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #1497141
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #1609924
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #1612737
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #1773166
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #1781794
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
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