6-hydroxy-nicotinic acid

O=C(OCc1ccccc1)c1ccc(O)nc1
Reaction #1731
benzyl 6-hydroxy-nicotinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[Si](C)(C)C/C=C/COC(=O)c1ccc(O)nc1
Reaction #1735
4-trimethylsilanyl-(E)-but-2-enyl 6-hydroxy-nicotinate
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCn1c(=O)c2[nH]c(-c3ccc(Cl)nc3)nc2n(CCC)c1=O
Reaction #42898
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(Br)nc1
Reaction #65635
methyl 6-bromo-nicotinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(O)c1cnc(O)c(Br)c1
Reaction #78082
6-hydroxy-5-bromonicotinic acid
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)c1ccc(O)nc1
Reaction #92953
6-hydroxy nicotinic acid
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(O)c1cnc(O)c(Br)c1
Reaction #169447
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cccnc1CN(CCCNC(=O)c1ccc(O)nc1)C(C)c1ccccn1
Reaction #225027
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(O)nc1
Reaction #234880
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(O)nc1
Reaction #262991
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)CNC(=O)c1ccc(O)nc1
Reaction #274132
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cc(Br)c(=O)n(-c2ccccc2)c1
Reaction #316832
3-bromo-5-(methoxycarbonyl)-1-phenyl-1,2-dihydropyridin-2-one
Ausbeute 92.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)c1ccc(O)nc1
Reaction #336663
methyl 6-hydroxynicotinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
Cc1cnc(CN(CCCCNC(=O)c2ccc(O)nc2)[C@@H](C)c2ccccn2)c(C)c1
Reaction #338180
free base
Ausbeute 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cccnc1CN(CCCNC(=O)c1ccc(O)nc1)Cc1ncccc1C
Reaction #338271
free base
Ausbeute 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cccnc1CN(CCCNC(=O)c1ccc(O)nc1)C(C)c1ccccn1
Reaction #338280
free base
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cnc(CN(CCCCNC(=O)c2ccc(O)nc2)C2CCCc3cccnc32)c(C)c1
Reaction #338394
free base
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cccnc1CN(CCCNC(=O)c1ccc(O)nc1)Cc1ncccc1C
Reaction #370479
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cnc(OCC(=O)OC)c([N+](=O)[O-])c1
Reaction #402586
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN(c1ccccc1)c1nc(N)nc(-c2noc(-c3ccc(O)nc3)n2)n1
Reaction #428680
5-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)pyridin-2-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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