trans-1,2-cyclohexanediamine

CCOCc1nc2c(N)nc3cc(-n4cccn4)ccc3c2n1CCCOC
Reaction #9564
2-ethoxymethyl-1-(3-methoxypropyl)-7-(pyrazol-1-yl)-1H-imidazo[4,5-c]quinolin-4-amine
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)Cc1cccc(-n2cccn2)c1
Reaction #44062
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #45509
tri-acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cncnc2)CC1
Reaction #48153
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CS(=O)(=O)c1ccc(-n2cccn2)c(C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)c1
Reaction #61042
title compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1CCCN1c1ccc(Cl)cc1F
Reaction #68496
1-(4-chloro-2-fluorophenyl)pyrrolidin-2-one
Ausbeute 108.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1cnn(-c2ccccc2)c1
Reaction #68655
4-bromo-1-phenyl-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(Br)cc1CCc1c(Cl)cccc1C1=NC2CCCCC2N1
Reaction #75567
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc(-c2ccn(-c3cccc(C(F)(F)F)c3)n2)cc1Br
Reaction #157433
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)C(=O)Nc1ncccc1-n1cc(Br)cn1
Reaction #165065
title compound
Ausbeute 53.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1N(c2cccnc2)CCN1c1ccc2ccccc2c1
Reaction #167205
1-naphthalen-2-yl-3-pyridin-3-yl-imidazolidin-2-one
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCn1ccc2cc(N3CCN(c4cccnc4)C3=O)ccc21
Reaction #167206
product
Ausbeute 49.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1N(c2cccnc2)CCN1c1ccc2ncsc2c1
Reaction #167207
product
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCN1C(=O)CCc2cc(N3CCN(c4cccnc4)C3=O)ccc21
Reaction #167208
product
Ausbeute 47.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1c(N2CCN(c3cccnc3)C2=O)sc2ccc(F)cc12
Reaction #167209
product
Ausbeute 61.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1N(c2cccnc2)CCN1c1ccc2sccc2c1
Reaction #167210
product
Ausbeute 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1N(c2cccnc2)CCN1c1ccc2ncccc2c1
Reaction #167211
product
Ausbeute 60.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1N(c2cccnc2)CCN1c1ccc2scnc2c1
Reaction #167212
product
Ausbeute 61.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1N(c2cccnc2)CCCN1c1ccc2ccccc2c1
Reaction #167215
product
Ausbeute 35.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(Cl)nc2ccc(N3CCN(c4cccnc4)C3=O)cc12
Reaction #167216
product
Ausbeute 35.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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