pyridine-2-carbonyl chloride

—
Reaction #56981
solid
수율 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #56985
solid
수율 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(NCCO)c1ccccn1
Reaction #63228
N-(2-Hydroxyethyl)pyridine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C[C@H]1CNCCN1C(=O)c1ccccn1.Cl.Cl
Reaction #69581
title compound
수율 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@H]1CN(C(=O)c2ccccn2)CCN1S(=O)(=O)c1ccc(Cl)cc1.Cl
Reaction #69588
title compound
수율 72.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@@H]1CN(S(=O)(=O)c2ccc(Cl)cc2)CCN1C(=O)c1ccccn1
Reaction #69593
title compound
수율 45.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(OC1CCC(COC(=O)N2CCCC2)CC1)c1ccccn1
Reaction #155666
compound
수율 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1noc2ccccc12)N1CCN(C(=O)c2ccccn2)CC1
Reaction #173025
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCC(c2c[nH]c3ccc(NC(=O)c4ccccn4)nc23)CC1
Reaction #178059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #181793
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(=O)N1CCN(c2ccc(NC(=O)c3ccccn3)cc2Cl)CC1
Reaction #192247
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCc1cc(Br)ccc1NC(=O)c1ccccn1)c1ccccn1
Reaction #207613
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(Oc2ccc(C(=O)CNC(C)C)cc2OC(=O)c2ccccn2)cc1
Reaction #236687
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(CCCc1ccc(Cl)cc1)c1nc(NCCc2ccc(O)cc2)nc(N2CCN(C(=O)c3ccccn3)CC2)n1
Reaction #245609
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Nc1cc2nc(-c3ccc([N+](=O)[O-])cc3)[nH]c2cn1)c1ccccn1
Reaction #246883
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Nc1c[nH]c2ncc(C(F)(F)F)c(Cl)c12)c1ccccn1
Reaction #249384
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc2c(c1)CC(C)(C)C(c1ccc(NC(=O)c3ccccn3)cc1)N2
Reaction #272678
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CS(=O)(=O)c1ccc(Nc2ncnc(OC3CCN(C(=O)c4ccccn4)CC3)c2[N+](=O)[O-])cc1
Reaction #277661
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc2c(c1)CC(C)(C)C(c1ccc(NC(=O)c3ccccn3)cc1)N2
Reaction #283628
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#Cc1cc(Br)ccc1NC(=O)c1ccccn1
Reaction #294490
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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