1-ethynylcyclohexanamine

Cn1c(C#CC2(N)CCCCC2)nc(-c2ccccc2)c1-c1nc2c(N)ncnc2s1
Reaction #60890
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C#CC1(NCC(O)COc2ccc(NC(=O)C(C)C)cc2C#N)CCCCC1
Reaction #95398
1-[2-cyano-4-(isobutyroyl-amino)-phenoxy]-3-(1-ethinyl-cyclohexylamino)-2-propanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cn1c(C#CC2(N)CCCCC2)nc(-c2ccccc2)c1-c1nc2c(N)ncnc2s1
Reaction #237549
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CC1(NC(=O)C(CCN2CCN(c3ccccc3OC)CC2)c2ccccc2)CCCCC1
Reaction #288926
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC1(CCc2ccc(F)cc2)CCCCC1
Reaction #295459
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC1(CCc2ccc(F)cc2)CCCCC1
Reaction #316594
1-[2-(4-fluoro-phenyl)-ethyl]-cyclohexylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C#CC1(NCCCS(=O)(=O)O)CCCCC1
Reaction #326937
3-(1-ethynylcyclohexyl)amino-1-propanesulfonic acid
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C#CC1(NS(=O)(=O)c2cccc(Cl)c2)CCCCC1
Reaction #372761
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc2ccc(C#CC3(N)CCCCC3)cc2c(-c2ccc(Cl)cc2)c1C(OC(C)(C)C)C(=O)O
Reaction #601268
2-(7-((1-Aminocyclohexyl)ethynyl)-1-(4-chlorophenyl)-3-methylnaphthalen-2-yl)-2-tert-butoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
Cc1cc2ccc(C#CC3(N)CCCCC3)cc2c(-c2ccc(Cl)cc2)c1[C@H](OC(C)(C)C)C(=O)O
Reaction #601282
(S)-2-(7-((1-Aminocyclohexyl)ethynyl)-1-(4-chlorophenyl)-3-methylnaphthalen-2-yl)-2-tert-butoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
C#CC1(NC(=O)NC)CCCCC1
Reaction #726627
1-(1-ethynyl-cyclohexyl)-3-methylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
C#CC1(NS(=O)(=O)c2cccc(Cl)c2)CCCCC1
Reaction #744865
title compound
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
C#CC1(NS(=O)(=O)c2cccc(Cl)c2)CCCCC1
Reaction #1129248
title compound
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
C#CC1(NS(=O)(=O)c2cccc(Cl)c2)CCCCC1
Reaction #1218780
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
C#CC1(NC(=O)NC)CCCCC1
Reaction #1643385
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
C#CC1(NC(=O)NC)CCCCC1
Reaction #2282173
1-(1-ethynyl-cyclohexyl)-3-methylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_12
C#CC1(NCCCS(=O)(=O)O)CCCCC1
Reaction #2306946
3-(1-ethynylcyclohexyl)amino-1-propanesulfonic acid
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_08
CCC1(N=C=S)CCCCC1
Reaction #2373302
1-isothiocyano-1-ethyl-cyclohexane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_04
C#CC1(NC(=O)C(CCN2CCN(c3ccccc3OC)CC2)c2ccccc2)CCCCC1
Reaction #2486883
title compound
Ausbeute 31.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_09