cyclohexylamine

Cc1cccnc1NC1CCCCC1
Reaction #713
Ausbeute 61.8%750 AstraZeneca ELN dataset
Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(NC3CCCCC3)nc21
Reaction #3293
2-Cyclohexylamino-6-(2,6-dichlorophenyl)-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NC(=S)NC1CCCCC1
Reaction #5128
Cyclohexylthiourea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=[N+]([O-])c1cccnc1NC1CCCCC1
Reaction #11381
N-Cyclohexyl-3-nitro-2-pyridineamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)CCNC1CCCCC1
Reaction #40626
title compound
Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCC(=O)N[C@H](C(=O)NC1CCCCC1)C(C)C
Reaction #42003
N-lauroyl-L-valine cyclohexylamide
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCC(=O)N[C@H](C(=O)NC1CCCCC1)C(C)C
Reaction #43895
N-lauroyl-L-valine cyclohexylamide
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C([O-])C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O.[NH-]C1CCCCC1
Reaction #46175
title compound
Ausbeute 59.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(NC1CCCCC1)C1=C(c2ccccc2)c2ccc(O)cc2C1=O
Reaction #47833
titled compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NC1CCCCC1
Reaction #47844
titled compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc2ncc(NC3CCCCC3)nc2cc1OC
Reaction #51616
product
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc2ncc(CNC3CCCCC3)nc2cc1OC
Reaction #51622
Cyclohexyl-(6,7-dimethoxyquinoxalin-2-ylmethyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=[N+]([O-])c1ccc(-c2cnc(NC3CCCCC3)s2)cc1
Reaction #51634
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(NC1CCCCC1)c1n[nH]c2ccc([N+](=O)[O-])cc12
Reaction #53673
N-cyclohexyl-5-nitro-1H-indazole-3-carboxamide
Ausbeute 459.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCC=C1CCCCC1N
Reaction #55513
1-BUTYLIDENE CYCLOHEXYLAMINE
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cc1ccc(C(=O)NC2CC2)cc1-c1ccc(-c2nnc(CNC3CCCCC3)o2)cc1
Reaction #59760
4′-{5-[(Cyclohexylamino)methyl]-1,3,4-oxadiazol-2-yl}-N-cyclopropyl-6-methyl-1,1′-biphenyl-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=C(C(=O)NC1CCCCC1)c1ccccc1
Reaction #65645
product
Ausbeute 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(NC1CCCCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67841
N-cyclohexyl-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1C=C(NC2CCCCC2)C(c2ccccc2)N1c1ccc2[nH]cnc2c1
Reaction #70048
1-(1H-Benzo[d]imidazol-5-yl)-4-(cyclohexylamino)-5-phenyl-1H-pyrrol-2(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1C=C(NC2CCCCC2)C(c2ccc(N3CCOCC3)cc2)N1c1ccc2[nH]cnc2c1
Reaction #70049
1-(1H-Benzo[d]imidazol-5-yl)-4-(cyclohexylamino)-5-(4-morpholinophenyl)-1H-pyrrol-2(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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