ethyl 5-bromopyridine-3-carboxylate

CCOC(=O)c1cncc(N2CCOCC2)c1
Reaction #334
Ausbeute 0.0%750 AstraZeneca ELN dataset
CCOC(=O)c1cncc(N2CCOCC2)c1
Reaction #335
Ausbeute 0.0%750 AstraZeneca ELN dataset
CCOC(=O)c1cncc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #72033
title compound
Ausbeute 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N[C@@]1(C(=O)O)CN(c2cncc(C(=O)O)c2)C[C@@H]1CCCB(O)O
Reaction #89649
5-((3R,4S)-3-amino-4-(3-boronopropyl)-3-carboxypyrrolidin-1-yl)nicotinic acid
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1cncc(-c2cnn3cc(-c4ccc(OC)cc4)cnc23)c1
Reaction #188450
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1cncc(N2C[C@H]3CN(C(=O)OC(C)(C)C)C[C@H]3C2)c1
Reaction #327685
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCOC(=O)c1cncc(Cc2ccccc2)c1
Reaction #340282
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCOC(=O)c1cncc(-c2ccccc2-c2ccccc2OCc2ccccc2)c1
Reaction #356769
colourless gum
Ausbeute 80.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
OCc1cncc(Br)c1
Reaction #370101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cncc(-c2ccc(C(C)C)cc2)c1
Reaction #371084
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cncc(-c2ccccc2-c2ccccc2OCc2ccccc2)c1
Reaction #381695
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cncc(-c2ccc(C)cc2F)c1
Reaction #388296
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cncc(-c2c(F)cccc2F)c1
Reaction #395302
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cncc(-c2ccc(CC)cc2)c1
Reaction #402161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cncc(Sc2ccc(NC(=O)C(C)(O)C(F)(F)F)c(Cl)c2)c1
Reaction #403268
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
OCc1cncc(Br)c1
Reaction #406764
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(O)c1cncc(Br)c1
Reaction #438921
3-bromo-5-(1-hydroxy-1-methylethyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CCOC(=O)c1cncc(C#Cc2ccccc2)c1
Reaction #478690
title compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCOC(=O)c1cncc(-c2cc(OC)c(OC)c(OC)c2)c1
Reaction #482626
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
Cl.OCc1cncc(Br)c1
Reaction #485094
(5-Bromo-pyridin-3-yl)-methanol Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
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