1-azabicyclo[2.2.2]oct-3-ylacetic acid hydrochloride

Cl.O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #84050
Pentafluorophenyl (1-azabicyclo[2.2.2]oct-3-yl)acetate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(C(=O)O)c(F)c1F
Reaction #84051
polymer-bound title compound
Выход 235.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cl.O=C(CC1CN2CCC1CC2)Nc1ccc2cccc([N+](=O)[O-])c2c1
Reaction #84054
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cl.O=C(CC1CN2CCC1CC2)Nc1cccc(Br)c1
Reaction #809355
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
Cl.O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #1553172
Pentafluorophenyl (1-azabicyclo[2.2.2]oct-3-yl)acetate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(C(=O)O)c(F)c1F
Reaction #1553173
polymer-bound title compound
Выход 235.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
Cl.O=C(CC1CN2CCC1CC2)Nc1ccc2cccc([N+](=O)[O-])c2c1
Reaction #1553176
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
Cl.O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #1983672
Pentafluorophenyl (1-azabicyclo[2.2.2]oct-3-yl)acetate Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(C(=O)O)c(F)c1F
Reaction #1983673
polymer-bound title compound
Выход 235.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
Cl.O=C(CC1CN2CCC1CC2)Nc1ccc2cccc([N+](=O)[O-])c2c1
Reaction #1983675
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
Cl.O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #2075036
Pentafluorophenyl (1-azabicyclo[2.2.2]oct-3-yl)acetate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(C(=O)O)c(F)c1F
Reaction #2075037
polymer-bound title compound
Выход 235.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
Cl.O=C(CC1CN2CCC1CC2)Nc1ccc2cccc([N+](=O)[O-])c2c1
Reaction #2075040
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
CC(C)(NC(=O)CC1CN2CCC1CC2)c1ccc(Br)cc1
Reaction #2362093
N-(2-(4-bromophenyl)propan-2-yl)-2-(quinuclidin-3-yl)acetamide
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
CC(C)(NC(=O)CC1CN2CCC1CC2)c1ccc(Br)cc1
Reaction #2368432
N-(2-(4-bromophenyl)propan-2-yl)-2-(quinuclidin-3-yl)acetamide
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09