2-Hydroxynicotinic acid

O=C(O)c1cc(Br)cnc1O
Reaction #4891
product
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCOC(=O)c1cccnc1Cl
Reaction #6523
ethyl 2-chloronicotinate
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
OCc1cccnc1O
Reaction #7263
alcohol
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=c1[nH]cccc1CO
Reaction #172375
3-(Hydroxymethyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)c1cc(Cl)cnc1O
Reaction #188896
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1cc(Cl)cnc1O
Reaction #205633
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1cc(Br)cnc1O
Reaction #234079
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cccnc1O
Reaction #250989
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cccnc1O
Reaction #271937
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)COc1c(C(=O)OC)sc(-c2cccc(NC(=O)c3cccnc3O)c2)c1Br
Reaction #281049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cc(Br)cn(-c2ccccc2)c1=O
Reaction #316834
5-bromo-3-methoxycarbonyl-1-phenyl-1,2-dihydropyridin-2-one
Ausbeute 60.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(O)c1cc(Br)cnc1O
Reaction #323319
product
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
O=C(O)c1cc(Br)cnc1O
Reaction #325666
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(O)c1cc(Br)cnc1O
Reaction #334445
product
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
CC(=O)OC(C)(C)c1cccnc1CN(CCCCNC(=O)c1ccc(O)nc1)Cc1ncc(C)cc1C
Reaction #338225
acetic acid 1-{2-[((3,5-dimethyl-pyridin-2-ylmethyl)-{4-[(6-hydroxy-pyridine-3-carbonyl)-amino]-butyl}-amino)-methyl]-pyridin-3-yl}-1-methyl-ethyl ester
Ausbeute 38.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=C(O)c1cc([N+](=O)[O-])cnc1O
Reaction #401566
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)c1cc([N+](=O)[O-])cnc1O
Reaction #408004
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Nc1ccc(Oc2ccnc3[nH]ccc23)c(F)c1)c1ccc[nH]c1=O
Reaction #434738
desired product
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
O=C(O)c1cc(S(=O)(=O)O)cnc1O
Reaction #435602
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
O=C(O)c1cc(Br)cnc1O
Reaction #451555
product
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
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