#4523898

COC(=O)c1ccc(C(=O)N2CCN(c3ncccc3[N+](=O)[O-])CC2)nc1
Reaction #285503
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1cccnc1N1CCNCC1
Reaction #288807
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1cccnc1N1CCNCC1
Reaction #413666
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
COC(=O)c1ccc(C(=O)N2CCN(c3ncccc3[N+](=O)[O-])CC2)nc1
Reaction #468527
desired compound
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Nc1cccnc1N1CCNCC1
Reaction #527426
1-(3-amino-2-pyridyl)piperazine
Rendement 95.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
O=C(OCc1ccccc1)N1CCN(c2ncccc2[N+](=O)[O-])CC1
Reaction #749372
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(OCc1ccccc1)N1CCN(c2ncccc2[N+](=O)[O-])CC1
Reaction #951603
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_10
Nc1cccnc1N1CCNCC1
Reaction #980172
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_06
Nc1cccnc1N1CCNCC1
Reaction #1069708
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_02
Nc1cccnc1N1CCNCC1
Reaction #1197099
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_06
O=C(OCc1ccccc1)N1CCN(c2ncccc2[N+](=O)[O-])CC1
Reaction #1536902
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
Nc1cccnc1N1CCNCC1
Reaction #1769538
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_12
Nc1cccnc1N1CCNCC1
Reaction #1807949
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_04
Nc1cccnc1N1CCNCC1
Reaction #1856637
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_01
Nc1cccnc1N1CCNCC1
Reaction #1856700
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_01
Nc1cccnc1N1CCNCC1
Reaction #1857079
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_01
Nc1cccnc1N1CCNCC1
Reaction #2297072
3-amino-2-(1-piperazinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_10
O=C(OCc1ccccc1)N1CCN(c2ncccc2[N+](=O)[O-])CC1
Reaction #2380932
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11
Nc1cccnc1N1CCNCC1
Reaction #2381171
1-(3-amino-2-pyridyl)piperazine
Rendement 95.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11
Nc1cccnc1N1CCNCC1
Reaction #2412626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
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