(2,6-Dichlorophenyl)hydrazine hydrochloride

Clc1cccc(Cl)c1-n1cc2c(n1)-c1cccnc1Nc1ccncc1-2
Reaction #162425
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)c1nn(-c2c(Cl)cccc2Cl)c(N)c1C#N
Reaction #440611
pyrazole
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CC(C)c1nn(-c2c(Cl)cccc2Cl)c(N)c1C#N
Reaction #594916
pyrazole
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
N#Cc1cnn(-c2c(Cl)cccc2Cl)c1N
Reaction #742297
product
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Clc1cccc(Cl)c1-n1cc2c(n1)-c1cccnc1Nc1ccncc1-2
Reaction #1130675
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
N#Cc1cnn(-c2c(Cl)cccc2Cl)c1N
Reaction #1185446
product
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CC(C)c1nn(-c2c(Cl)cccc2Cl)c(N)c1C#N
Reaction #1453535
pyrazole
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
NNc1c(Cl)cccc1Cl
Reaction #1525050
2,6-dichloro-phenylhydrazine
Ausbeute 101.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
COC(=O)c1c(C(C)C)cnn1-c1c(Cl)cccc1Cl
Reaction #1776939
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
CCOC(=O)c1c(C2CC2)cnn1-c1c(Cl)cccc1Cl
Reaction #1776940
title compound
Ausbeute 37.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
CC(C)c1nn(-c2c(Cl)cccc2Cl)c(N)c1C#N
Reaction #1908626
pyrazole
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
CC(C)c1nnc2ccc(-c3cn(-c4c(Cl)cccc4Cl)nc3-c3ccc(F)cc3F)nn12
Reaction #2017169
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
CCOC(=O)c1c[nH]n(-c2c(Cl)cccc2Cl)c1=O
Reaction #2183004
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CSc1ncc2c(=O)n(-c3c(Cl)cccc3Cl)nc(-c3cccc(Cl)n3)c2n1
Reaction #2259569
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
CSc1ncc2c(=O)n(-c3c(Cl)cccc3Cl)nc(-c3cccc(Cl)n3)c2n1
Reaction #2259572
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
CCOC(=O)c1nn(-c2c(Cl)cccc2Cl)nc1COc1ccccc1
Reaction #2300723
2-(2,6-Dichloro-phenyl)-5-phenoxymethyl-2H-[1,2,3]triazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_09
CCOC(=O)c1c(CC(C)C)c(C)nn1-c1c(Cl)cccc1Cl
Reaction #2348919
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
CCOC(=O)c1c(C2CC2)cnn1-c1c(Cl)cccc1Cl
Reaction #2348920
title compound
Ausbeute 37.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
COC(=O)c1c(C(C)C)cnn1-c1c(Cl)cccc1Cl
Reaction #2348922
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
CSc1ncc2c(=O)n(-c3c(Cl)cccc3Cl)nc(-c3cccc(Cl)n3)c2n1
Reaction #2490132
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_08
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