quinuclidin-3-one hydrochloride

Clc1cccc(NCCNC2CN3CCC2CC3)c1
Reaction #5046
desired product
Ausbeute 3.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #43655
yellow solid
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #59352
alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #59358
yellow solid
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #72934
alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #72940
yellow solid
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #73558
yellow solid
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #73562
2-((3-pyridinyl)methylene)-1-azabicyclo[2.2.2]octan-3-one
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1CN2CCC1CC2
Reaction #84048
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #169603
yellow solid
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #169608
2-((3-pyridinyl)methylene)-1-azabicyclo[2.2.2]octan-3-one
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
ON=C1C2CCN(CC2)C1CN1CCCCC1
Reaction #414565
voluminous white needles
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
ON=C1C2CCN(CC2)C1CN1CCCC1
Reaction #414566
fine colorless needles
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
c1ccc(NC2CN3CCC2CC3)cc1
Reaction #436393
N-Phenyl-1-azabicyclo[2.2.2]octan-3-amine
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
—
Reaction #586088
alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #586094
yellow solid
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
—
Reaction #747189
alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #747195
yellow solid
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Cc1nnc(NCCNC2CN3CCC2CC3)c2cc3ccccn3c12
Reaction #791263
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_01
O=C1CN2CCC1CC2
Reaction #809352
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
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