5-bromopyridin-3-ylamine

Nc1cncc(N2CCOCC2)c1
Reaction #213
Yield 0.0%750 AstraZeneca ELN dataset
Nc1cncc(N2CCOCC2)c1
Reaction #214
Yield 0.0%750 AstraZeneca ELN dataset
CC1(C)OC(=O)C(C=Nc2cncc(Br)c2)C(=O)O1
Reaction #73062
5-{[(5-bromopyridin-3-yl)imino]methyl}-2,2-dimethyl-1,3-dioxane-4,6-dione
Yield 300.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)C(=O)Nc1cncc(Br)c1
Reaction #90367
N-(5-bromopyridin-3-yl)isobutyramide
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CN1CCC(C(=O)Nc2cncc(Br)c2)CC1
Reaction #90368
N-(5-bromopyridin-3-yl)-1-methylpiperidine-4-carboxamide
Yield 47.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)C(=O)Nc1cncc(Br)c1
Reaction #156108
N-(5-bromopyridin-3-yl)isobutyramide
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C)OC(=O)C(C=Nc2cncc(Br)c2)C(=O)O1
Reaction #169082
5-{[(5-bromopyridin-3-yl)imino]methyl}-2,2-dimethyl-1,3-dioxane-4,6-dione
Yield 300.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)C(=O)Nc1cncc(Br)c1
Reaction #169251
N-(5-bromopyridin-3-yl)isobutyramide
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN1CCC(C(=O)Nc2cncc(Br)c2)CC1
Reaction #169252
N-(5-bromopyridin-3-yl)-1-methylpiperidine-4-carboxamide
Yield 47.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCS(=O)(=O)Nc1cncc(Br)c1
Reaction #173465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)C(=O)Nc1cncc(Br)c1
Reaction #268937
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)(Nc1cncc(Br)c1)c1ccc(F)cc1
Reaction #280867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CS(=O)(=O)Nc1cncc(Br)c1
Reaction #294370
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1cncc(-c2ccccc2)c1
Reaction #337209
5-phenylpyridin-3-amine
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COc1ccc(CNc2cncc(Br)c2)cc1OC1CCCC1
Reaction #341970
5-bromo-N-(3-(cyclopentyloxy)-4-methoxybenzyl)pyridin-3-amine
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
—
Reaction #356441
solid
Yield 9.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCC(=O)Nc1cncc(Br)c1
Reaction #377617
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(CNc2cncc(Br)c2)cc1OC1CCCC1
Reaction #407848
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)C(=O)Nc1cncc(Br)c1
Reaction #421652
N-(5-bromopyridin-3-yl)pivalamide
Yield 73.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)Nc1cncc(Br)c1
Reaction #421654
5-bromo-N-isopropylpyridin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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