1-(2-pyridin-2-ylethyl)piperazine

CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #194
Ausbeute 35.8%750 AstraZeneca ELN dataset
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #195
Ausbeute 19.0%750 AstraZeneca ELN dataset
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #196
Ausbeute 46.9%750 AstraZeneca ELN dataset
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #197
Ausbeute 40.0%750 AstraZeneca ELN dataset
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #198
Ausbeute 69.5%750 AstraZeneca ELN dataset
O=C(c1cccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)c1)N1CCN(CCc2ccccn2)CC1
Reaction #243097
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(CCN2CCNCC2)nc1
Reaction #394902
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #470985
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
c1ccc(CCN2CCNCC2)nc1
Reaction #470996
1-[2-(2-Pyridyl)ethyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COc1cc(N2CCN(CCc3ccccn3)CC2)c2oc(C(=O)N(C)C)cc2c1
Reaction #471034
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #622814
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
c1ccc(CCN2CCNCC2)nc1
Reaction #622824
1-[2-(2-Pyridyl)ethyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COc1cc(N2CCN(CCc3ccccn3)CC2)c2oc(C(=O)N(C)C)cc2c1
Reaction #622862
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
N#CCN1CCN(CCc2ccccn2)CC1
Reaction #642947
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=C(c1cccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)c1)N1CCN(CCc2ccccn2)CC1
Reaction #746687
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1)N1CCN(CCc2ccccn2)CC1
Reaction #746739
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
O=C(Oc1ccc(Oc2ccc(C(F)(F)F)cn2)cc1)N1CCN(CCc2ccccn2)CC1
Reaction #757185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
N#CCN1CCN(CCc2ccccn2)CC1
Reaction #786223
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1)N1CCN(CCc2ccccn2)CC1
Reaction #1290295
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #1305538
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
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