2,5-dibromo-3-methylpyridine

CCOc1cccc(-c2ncc(Br)cc2C)c1
Reaction #70293
5-Bromo-2-(3-ethoxyphenyl)-3-methylpyridine
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cccc(-c2ncc(Br)cc2C)c1
Reaction #70297
5-Bromo-2-(3-methoxyphenyl)-3-methylpyridine
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(Br)cnc1Nc1ncc2c3ccncc3n(C3CCCC3)c2n1
Reaction #166301
N-(5-bromo-3-methyl-2-pyridinyl)-9-cyclopentyl-9H-pyrido[4′,3′:4,5]pyrrolo[2,3-d]pyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(Br)cnc1N1CCN(c2cc(-c3ccc(F)cc3)nc(N3CCCC3C)n2)C(C)C1
Reaction #199399
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Br)cnc1C#N
Reaction #427162
desired product
Yield 49.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1cc(Br)cnc1N1CC[C@@H](N(C)C)C1
Reaction #510578
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cc1cc(Br)cnc1C#N
Reaction #661301
50
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
Cc1cc(Br)cnc1N1CCNC(C)C1
Reaction #777198
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1cc(Br)cnc1N1CCC(N(C)C)C1
Reaction #886038
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cc1cc(Br)cnc1OC(C)C
Reaction #918918
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cc1cc(Br)cnc1Nc1ncc2c3ccncc3n(C3CCCC3)c2n1
Reaction #963132
N-(5-bromo-3-methyl-2-pyridinyl)-9-cyclopentyl-9H-pyrido[4′,3′:4,5]pyrrolo[2,3-d]pyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Cc1cc(Br)cnc1I
Reaction #1076001
5-bromo-2-iodo-3-methylpyridine
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_10
Cc1cc(Br)cnc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #1214048
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1cc(Br)cnc1I
Reaction #1253751
5-bromo-2-iodo-3-methylpyridine
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_09
Cc1cc(Br)cnc1I
Reaction #1444509
5-bromo-2-iodo-3-methylpyridine
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
Cc1cc(Br)cnc1I
Reaction #1445250
5-bromo-2-iodo-3-methylpyridine
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
CCC(CC)c1ccc(Cl)c2nc3n(c12)CCCCN3c1ncc(Br)cc1C
Reaction #1486408
1-(5-bromo-3-methylpyridin-2-yl)-10-chloro-7-(1-ethylpropyl)-2,3,4,5-tetrahydro-1H-[1,3]diazepino[1,2-a]benzimidazole
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Cc1cc(Br)cnc1N1CCN[C@H](C)C1
Reaction #1531290
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
Cc1cc(Br)cnc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #1531300
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
Cc1cc(Br)cnc1N1CCN(c2cc(-c3ccc(F)cc3)nc(N3CCC[C@H]3C)n2)[C@H](C)C1
Reaction #1531309
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
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