2-Methylnicotinic acid

Cc1ncccc1CO
Reaction #7264
alcohol
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1c(Cl)cc2c([nH]c3cnccc32)c1NC(=O)c1cccnc1C
Reaction #40458
desired product
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOc1c(Cl)cc2c([nH]c3cnccc32)c1NC(=O)c1cccnc1C
Reaction #40461
desired compound
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ncccc1C(=O)Nc1c(OCC2CC2)c(Cl)cc2c1[nH]c1cnccc12
Reaction #40474
desired compound
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ncccc1C(=O)Nc1c(F)c(Cl)cc2c1[nH]c1cnccc12
Reaction #40476
N-(6-chloro-7-fluoro-9H-β-carbolin-8-yl)-2-methyl-nicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSc1c(Cl)cc2c([nH]c3cnccc32)c1NC(=O)c1cccnc1C
Reaction #40478
N-(6-chloro-7-methylsulfanyl-9H-β-carbolin-8-yl)-2-methyl-nicotinamide
Yield 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCSc1c(Cl)cc2c([nH]c3cnccc32)c1NC(=O)c1cccnc1C
Reaction #40481
N-(6-chloro-7-ethylsulfanyl-9H-β-carbolin-8-yl)-2-methyl-nicotinamide
Yield 40.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ncccc1C(=O)Nc1cc(Cl)cc2c1[nH]c1cncc(NC(=O)C(F)(F)F)c12
Reaction #40493
N-[6-chloro-4-(2,2,2-trifluoro-acetylamino)-9H-β-carbolin-8-yl]-2-methyl-nicotinamide
Yield 33.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(Nc1cc(Cl)cc2c1[nH]c1cncc(NC(=O)C(F)(F)F)c12)c1cccnc1
Reaction #40494
N-[6-chloro-4-(2,2,2-trifluoro-acetylamino)-9H-β-carbolin-8-yl]-nicotinamide
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ncccc1C(=O)N[C@@H](C)CN1CC(C)(C)OC[C@H]1C(=O)Nc1cc(Cl)cc2c1[nH]c1cnccc12
Reaction #40504
desired compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(CN1CC(C)(C)OCC1C(=O)Nc1cc(Cl)cc2c1[nH]c1cnccc12)NC(=O)c1cccnc1C
Reaction #40509
6,6-dimethyl-4-{2-[(2-methyl-pyridine-3-carbonyl)-amino]-butyl}-morpholine-3-carboxylic acid (6-chloro-9H-β-carbolin-8-yl)-amide
Yield 80.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ncccc1C(=O)NC(CN1CC(C)(C)OCC1C(=O)Nc1cc(Cl)cc2c1[nH]c1cnccc12)C(C)C
Reaction #40511
6,6-dimethyl-4-{3-methyl-2-[(2-methyl-pyridine-3-carbonyl)-amino]-butyl}-morpholine-3-carboxylic acid (6-chloro-9H-β-carbolin-8-yl)-amide
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ncccc1C(=O)N(Cc1cccc(-c2ccnc(NCCc3ccc(O)c(Cl)c3)n2)c1)C(C)C
Reaction #43192
N-(3-{2-[2-(3-Chloro-4-hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzyl)-N-isopropyl-2-methyl-nicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ncccc1C(=O)Cl
Reaction #71665
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ncccc1C(=O)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #71669
1-[(2-Methyl-3-pyridinyl)carbonyl]-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ncccc1C(=O)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)[C@H](C)C1.O=CO
Reaction #71674
title compound
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ncccc1C(=O)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)[C@@H](C)C1.O=CO
Reaction #71676
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ncccc1C(=O)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)C[C@H]1C.O=CO
Reaction #71684
title compound
Yield 122.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ncccc1C(N)=O
Reaction #80642
2-methylnicotinamide
Yield 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCC(CN1CC(C)(C)OCC1C(=O)Nc1cc(Cl)cc2c1[nH]c1cnccc12)NC(=O)c1cccnc1C
Reaction #176470
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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