trans-4-methylamino-cyclohexanol

CN(C(=O)Oc1ccc(F)c(F)c1)[C@H]1CC[C@H](O)CC1
Reaction #53820
trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 3,4-difluoro-phenyl ester
Ausbeute 238.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](O)CC1
Reaction #53822
trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 4-chloro-phenyl ester
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN([C@H]1CC[C@H](O)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #53825
trans-N-(4-Hydroxy-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN([C@H]1CC[C@H](O)CC1)S(=O)(=O)c1ccc(Br)cc1
Reaction #53826
trans-4-Bromo-N-(4-hydroxy-cyclohexyl)-N-methyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cnc(N2CCOCC2)c2sc(NC(=O)N(C)[C@H]3CC[C@H](O)CC3)nc12
Reaction #1004621
Trans-1-(4-Hydroxy-cyclohexyl)-3-(7-methoxy-4-morpholin-4-yl-thiazolo[5,4-c]pyridin-2-yl)-1-methyl-urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COc1ccc(C2COCCO2)c2sc(NC(=O)N(C)[C@H]3CC[C@H](O)CC3)nc12
Reaction #1072995
(+)-trans-3-(7-[1,4]Dioxan-2-yl-4-methoxy-benzothiazol-2-yl)-1-(4-hydroxy-cyclohexyl)-1-methyl-urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
CN([C@H]1CC[C@H](O)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #1150803
trans-N-(4-hydroxy-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
CN(C(=O)Oc1ccc(F)c(F)c1)[C@H]1CC[C@H](O)CC1
Reaction #2144400
trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 3,4-difluoro-phenyl ester
Ausbeute 238.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_02
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](O)CC1
Reaction #2144402
trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 4-chloro-phenyl ester
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_02
CN([C@H]1CC[C@H](O)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #2144405
trans-N-(4-Hydroxy-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_02
CN([C@H]1CC[C@H](O)CC1)S(=O)(=O)c1ccc(Br)cc1
Reaction #2144406
trans-4-Bromo-N-(4-hydroxy-cyclohexyl)-N-methyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_02