2-Chloropyridine

CCOC(=O)c1cnc(Nc2ccccn2)o1
Reaction #585
Ausbeute 37.8%750 AstraZeneca ELN dataset
c1ccc(Nc2ncco2)nc1
Reaction #672
Ausbeute 0.0%750 AstraZeneca ELN dataset
c1ccc(Nc2ncco2)nc1
Reaction #673
Ausbeute 0.0%750 AstraZeneca ELN dataset
c1ccc(Nc2ncco2)nc1
Reaction #674
Ausbeute 0.0%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)N1CCC[C@@H](Nc2ccccn2)C1
Reaction #697
Ausbeute 93.4%750 AstraZeneca ELN dataset
C[C@H](O)CNc1ccccn1
Reaction #992
title compound
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccccc1-c1ccccn1
Reaction #42149
2-ortho-tolylpyridine
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccccc1-c1ccccn1
Reaction #42166
2-ortho-tolylpyridine
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN1CCC(C(=O)c2cccc(Cl)n2)CC1
Reaction #58482
title product
Ausbeute 47.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
NC(=O)c1ccc(-c2ccnc(NCCNc3ccccn3)n2)cc1
Reaction #60019
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccccc1
Reaction #60190
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccc(Cl)cc1Cl
Reaction #60191
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccc(C#N)cc1
Reaction #60192
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCO[C@@H]1CN(c2ccccn2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71996
title compound
Ausbeute 3.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1ccc(Sc2ccccn2)cc1
Reaction #83375
2-(4-aminophenylthio)pyridine
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(O)c1cccnc1Cl
Reaction #90352
1-(2-chloropyridin-3-yl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(O)c1cccnc1Cl
Reaction #90356
1-(2-chloropyridin-3-yl)ethanol
Ausbeute 38.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCC1CN(c2ccccn2)CC2(CCN(C(=O)OC(C)(C)C)CC2)O1
Reaction #160083
tert-butyl 10-ethyl-8-(2-pyridyl)-11-oxa-3,8-diazaspiro[5.5]undecane-3-carboxylate
Ausbeute 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(O)c1cccnc1Cl
Reaction #169236
1-(2-chloropyridin-3-yl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(O)c1cccnc1Cl
Reaction #169240
1-(2-chloropyridin-3-yl)ethanol
Ausbeute 38.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Seite 1Weiter