trans-4-(aminomethyl)cyclohexanecarboxylic acid

COC(=O)[C@H]1CC[C@H](CN)CC1.Cl
Reaction #44975
methyl trans-4-(aminomethyl)-cyclohexanecarboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)NC[C@H]1CC[C@H](C(=O)O)CC1
Reaction #166048
trans-{4-[(acetylamino) methyl]cyclohexyl}carboxylic acid
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)[C@H]1CC[C@H](CN)CC1.Cl
Reaction #218454
methyl trans-4-(aminomethyl)cyclohexanecarboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(NC[C@H]1CC[C@H](C(=O)O)CC1)OCc1ccccc1
Reaction #332920
(trans)-4-((benzyloxycarbonylamino)methyl)cyclohexanecarboxylic acid
Ausbeute 92.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(NC[C@H]1CC[C@H](C(=O)O)CC1)OCc1ccccc1
Reaction #350615
trans-4-(N-carbobenzyloxy)aminomethyl-1-cyclohexane carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Cc1ccc(S(=O)(=O)O)cc1.NC[C@H]1CC[C@H](C(=O)OCc2ccccc2)CC1
Reaction #351186
trans-4-(aminomethyl)-cyclohexane carboxylic acid benzyl ester para-toluenesulfonate salt
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Cl.NC[C@H]1CC[C@H](CO)CC1
Reaction #409676
trans-4-(Aminomethyl)cyclohexanemethanol hydrochloride
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCn1ncc2c(NCC3CCC(C(=O)OCSC)CC3)c3ccccc3nc21
Reaction #463032
1-ethyl-N-[[4-(methylthiomethoxycarbonyl) cyclohexyl]methyl]-1H-pyrazolo[3,4-b]quinolin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
Cl.NC[C@H]1CC[C@H](CO)CC1
Reaction #464275
trans-4-(Aminomethyl)cyclohexanemethanol hydrochloride
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
O=C(O)[C@H]1CC[C@H](CN=C=S)CC1
Reaction #472372
trans-4-(isothiocyanatomethyl)cyclohexanecarboxylic acid
Ausbeute 101.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)CC(=O)OCOC(=O)NC[C@H]1CC[C@H](C(=O)O)CC1
Reaction #474114
title compound 5
Ausbeute 49.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)(C)C(=O)OCOC(=O)C(N)[C@H]1CC[C@H](C(=O)O)CC1
Reaction #474115
title compound 6
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(NC[C@H]1CC[C@H](C(=O)O)CC1)OCOC(=O)c1ccccc1
Reaction #474116
title compound 7
Ausbeute 66.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(=O)OC(C)OC(=O)NC[C@H]1CC[C@H](C(=O)O)CC1
Reaction #474117
title compound 8
Ausbeute 22.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCC(=O)OC(C)OC(=O)NC[C@H]1CC[C@H](C(=O)O)CC1
Reaction #474118
title compound 9
Ausbeute 7.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCCC(=O)OC(C)OC(=O)NC[C@H]1CC[C@H](C(=O)O)CC1
Reaction #474119
title compound 10
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCCC(=O)OC(C)OC(=O)NC[C@H]1CC[C@H](C(=O)[O-])CC1.[Na+]
Reaction #474120
title compound 11
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCCCC(=O)OC(C)OC(=O)NC[C@H]1CC[C@H](C(=O)O)CC1
Reaction #474121
title compound 12
Ausbeute 16.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(OC(=O)C(C)C)OC(=O)C(N)[C@H]1CC[C@H](C(=O)O)CC1
Reaction #474122
title compound 13
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(OC(=O)C(C)C)OC(=O)C(N)[C@H]1CC[C@H](C(=O)[O-])CC1.[Na+]
Reaction #474123
title compound 14
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Seite 1Weiter