6-chloronicotinic acid

CCOC(=O)c1ccc(Cl)nc1
Reaction #1319
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc(I)nc1
Reaction #1320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(Cl)nc1
Reaction #6081
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1ccc(Cl)nc1
Reaction #6655
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)N1CCN(C(=O)c2ccc(Cl)nc2)CC1
Reaction #58742
title compound
収率 111.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)c1ccc(Cl)nc1
Reaction #64626
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
NNc1ccc(C(=O)O)cn1
Reaction #65723
pale brown solid
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CON(C)C(=O)c1ccc(Cl)nc1
Reaction #67725
6-chloro-N-methoxy-N-methyl-nicotinamide
収率 46.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cl.O=C(Cl)c1ccc(Cl)nc1
Reaction #70835
desired product
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@H]1CN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CCN1C(=O)c1ccc(Cl)nc1
Reaction #71690
title compound
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(c1ccc(Cl)nc1)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #71704
title compound
収率 49.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1ccc(Cl)nc1
Reaction #80649
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1ccc(Cl)nc1
Reaction #81592
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)c1ccc(I)nc1
Reaction #81593
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1ccc(Cl)nc1
Reaction #81656
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)c1ccc(I)nc1
Reaction #81657
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #93804
1a
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CN1CCN(C(=O)c2ccc(Cl)nc2)CC1
Reaction #155626
(6-Chloro-pyridin-3-yl)-(4-methyl-piperazin-1-yl)-methanone
収率 49.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)c1ccc(Cl)[n+]([O-])c1
Reaction #181242
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(CNC(=O)c2ccc(Cl)nc2)C1
Reaction #188507
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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