Impliqué dans 43 réactions

14512

CCOC(=O)c1c(C)nn(C2CCCCC2)c1C
Reaction #8162
1-cyclohexyl-3,5-dimethyl-1H-pyrazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cnn(C2CCCCC2)c1N
Reaction #41156
5-amino-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester
Rendement 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1cnn(C2CCCCC2)c1C(F)(F)F
Reaction #41171
1-cyclohexyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester
Rendement 58.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1cnn(C2CCCCC2)c1N
Reaction #487671
5-Amino-1-cyclohexyl-1H-pyrazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCOC(=O)c1c(C)nn(C2CCCCC2)c1C
Reaction #500948
1-Cyclohexyl-3,5-dimethyl-1H-pyrazole-4-carboxylic Acid Ethyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CC1=NN(C2CCCCC2)C(=O)C1
Reaction #635956
titled compound
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
Cc1cc(-c2c(C)nn(-c3ccccc3)c2O)n(C2CCCCC2)n1
Reaction #642819
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cn1c(=O)c(-c2ccc(Cl)cc2Cl)cc2c3cc(-c4ccnn4C4CCCCC4)ccc3n(C)c21
Reaction #646422
6-(2-Cyclohexyl-2H-pyrazol-3-yl)-3-(2,4-dichlorophenyl)-1,9-dimethyl-1,9-dihydropyrido[2,3-b]indol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CC(C)(C)c1cc(N)n(C2CCCCC2)n1.Cl
Reaction #718865
3-tert-butyl-1-cyclohexyl-1H-pyrazol-5-amine hydrochloride
Rendement 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CC(C)(C)c1cc(N)n(C2CCCCC2)n1.Cl
Reaction #958913
3-tert-butyl-1-cyclohexyl-1H-pyrazol-5-amine hydrochloride
Rendement 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Clc1cc2c(cn1)-c1nc(-c3ncnn3C3CCCCC3)cn1CCO2
Reaction #973600
8-Chloro-2-(2-cyclohexyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a,9-triaza-benzo[e]azulene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CC1=NN(C2CCCCC2)C(=O)C1
Reaction #1003089
captioned compound
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
Oc1cc(COC23CC4CC(CC(C4)C2)C3)nn1C1CCCCC1
Reaction #1054982
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_10
CCOC(=O)c1cnn(C2CCCCC2)c1N
Reaction #1111778
5-Amino-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
Oc1ccc(-c2nn(C3CCCCC3)c3cc(O)ccc23)c(O)c1
Reaction #1382061
product
Rendement 24.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
COc1ccc(-c2nn(C3CCCCC3)c3c(Cl)cccc23)cc1
Reaction #1382079
product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
COc1ccc(-c2nn(C3CCCCC3)c3c(C(F)(F)F)cccc23)cc1
Reaction #1382083
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
COc1ccc(-c2nn(C3CCCCC3)c3c(F)cccc23)cc1
Reaction #1382085
title compound
Rendement 46.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
CC1=NN(C2CCCCC2)C(=O)C1
Reaction #1485273
title compound
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Cc1cc(=O)n(C2CCCCC2)[nH]1
Reaction #1565391
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
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