2-bromo-5-methylpyridine

COc1cc(-c2nc3ccccc3o2)ccc1-c1ncccc1C
Reaction #7881
2-[3-methoxy-4-(3-methylpyridin-2-yl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(NC[C@@H]2[C@H](C)CCCN2C(=O)c2cc(C)ccc2-n2nccn2)nc1
Reaction #89245
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(NC[C@@H]2[C@H](C)CCCN2C(=O)c2cc(C)ccc2-n2cnc(C)n2)nc1
Reaction #89252
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(NC[C@@H]2[C@H](C)CCCN2C(=O)c2cc(C)ccc2-n2cnc(C(F)(F)F)n2)nc1
Reaction #89254
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(NC[C@@H]2[C@H](C)CCCN2C(=O)c2cc(C)ccc2-c2ccccn2)nc1
Reaction #89258
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(NC[C@@H]2[C@H](C)CCCN2C(=O)c2cc(C)ccc2-c2ccnn2C)nc1
Reaction #89262
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-c2ccc(C)cc2C(=O)O)nc1
Reaction #89320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(NC[C@@H]2[C@H](C)CCCN2C(=O)c2cc(C)ccc2-c2ncccn2)nc1
Reaction #89343
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(NC[C@@H]2[C@H](C)CCCN2C(=O)c2nc(C)ccc2-n2nccn2)nc1
Reaction #89403
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
BrCc1ccc(Br)nc1
Reaction #158850
2-bromo-5-bromomethylpyridine
Rendimiento 105.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(-c2ccc(C)cn2)cc([N+](=O)[O-])c1
Reaction #164928
3-(5-Methyl-pyridin-2-yl)-5-nitro-benzoic acid methyl ester
Rendimiento 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(Br)cc(-c2ccc(C)cn2)c1
Reaction #164944
3-bromo-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester
Rendimiento 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(-c2ccc(C=O)cc2)nc1
Reaction #171221
title compound
Rendimiento 122.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(-c2ccc(C)cn2)cc([N+](=O)[O-])c1
Reaction #171906
3-(5-Methyl-pyridin-2-yl)-5-nitro-benzoic acid methyl ester
Rendimiento 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(CC#N)nc1
Reaction #180754
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(-c2c(C)c(NC(=O)CC(C)(C)C)c(C)c3c2OCC3c2ccc(C(C)C)cc2)nc1
Reaction #186293
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
BrCc1ccc(Br)nc1
Reaction #251090
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(-c2ccc([Si](C)(C)C)cc2)nc1
Reaction #287005
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(N2CCC(NC(=O)OC(C)(C)C)CC2)nc1
Reaction #290955
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(F)(F)c1ccc(C)cn1
Reaction #294017
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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