methyl-5-hydroxypyridine-3-carboxylate

COC(=O)c1cncc(Oc2ccc([N+](=O)[O-])cc2)c1
Reaction #41779
methyl-5-(4-nitrophenoxy)pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cnc(I)c(O)c1
Reaction #171766
methyl 5-hydroxy-6-iodonicotinate
المردود 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cncc(OCCCCc2ncnc3scc(-c4ccc(F)cc4)c23)c1
Reaction #187953
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cncc(OC(=O)Oc2ccc([N+](=O)[O-])cc2)c1
Reaction #227036
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cncc(OC(C)C)c1
Reaction #259563
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cncc(O)c1
Reaction #271059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cncc(OCc2nc(-c3ccccc3)oc2C)c1
Reaction #437132
methyl 5-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridinecarboxylate
المردود 59.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(OC)nc1
Reaction #439363
6-methoxynicotinic acid methyl ester
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
COC(=O)[C@@H]1CNC[C@H](O)C1
Reaction #470966
methyl cis-5-hydroxypiperidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Oc1cncc(-c2nc(-c3ccccn3)no2)c1
Reaction #519093
3-(2-pyridyl)-5-(5-hydroxy-pyrid-3-yl)-1,2,4-oxadiazole
المردود 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
COC(=O)c1cncc(OC(=O)Oc2ccc([N+](=O)[O-])cc2)c1
Reaction #692983
methyl 5-{[(4-nitrophenoxy)carbonyl]oxy}nicotinate
المردود 76.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
COC(=O)c1cnc(I)c(O)c1
Reaction #715183
methyl 5-hydroxy-6-iodonicotinate
المردود 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
COC(=O)c1cncc(Oc2ccc([N+](=O)[O-])c(F)c2)c1
Reaction #745666
5-(4-nitro-3-fluorophenoxy)nicotinic acid methyl ester
المردود 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCC#CC(C)(C)NC(=O)C(CC)Oc1cncc(C(=O)OC)c1
Reaction #759310
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)c1cncc(Oc2ccc(C(C)=O)cc2Br)c1
Reaction #775615
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)c1cncc(OCc2cccc(OCc3nc(-c4ccccc4)oc3C)c2)c1
Reaction #789608
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)c1cncc(OCC(C)C)c1
Reaction #796941
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
—
Reaction #796956
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
COC(=O)c1cncc(OCc2ccccc2)c1
Reaction #913816
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)c1cncc(O)c1
Reaction #920679
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
الصفحة 1التالي