2-bromopyridine

c1ccc(N2CCC3(CC2)OCCO3)nc1
Reaction #332
Ausbeute 66.6%750 AstraZeneca ELN dataset
O=C(C1CC2(CCN(c3ccccn3)CC2)C1)N1CCN(C2CCC2)CC1
Reaction #780
Ausbeute 42.8%750 AstraZeneca ELN dataset
O=C(C1CC12CCN(c1ccccn1)CC2)N1CCN(C2CCC2)CC1
Reaction #827
Ausbeute 26.6%750 AstraZeneca ELN dataset
O=C(C1CC12CCN(c1ccccn1)CC2)N1CCN(C2CCC2)CC1
Reaction #828
Ausbeute 9.4%750 AstraZeneca ELN dataset
COc1cc(-c2nc3ccccc3o2)ccc1Cc1ccccn1
Reaction #7846
2-[3-methoxy-4-(pyridin-2-ylmethyl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #7877
EtOAc hexanes
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC#Cc1ccccn1
Reaction #9274
title compound
Ausbeute 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(C)cc(C)c1-c1cccc2c(Nc3ccccn3)c(SC)nn12
Reaction #9325
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc2c(c1)c(C)c(-c1ccccn1)n2C1CCCC1
Reaction #11514
Methyl 1-cyclopentyl-3-methyl-2-(2-pyridyl)indole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cccc(-c2ccccn2)c1
Reaction #44321
2-(3-methoxyphenyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(-c2ccccn2)cc1
Reaction #44322
2-(4-methoxy-phenyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(-c2ccccn2)c(F)c1
Reaction #44326
2-(2,4-difluorophenyl)pyridine
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #50215
solid
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Brc1ccc(-c2ccccn2)cc1
Reaction #51197
title product
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Nc1ccc(Cl)cc1C(=O)c1ccccn1
Reaction #57784
desired product
Ausbeute 45.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN(C)CCOc1ccc(-c2ccccn2)cc1C=O
Reaction #58895
title product
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(C(O)c3ccccn3)cc21
Reaction #60302
desired product
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=Cc1ccc(-c2ccccn2)cc1[N+](=O)[O-]
Reaction #66289
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(N)c1ccccn1
Reaction #67577
N-Methyl-N-pyridin-2-yl-hydrazine
Ausbeute 74.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCN(c1ccccn1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12
Reaction #69559
title compound
Ausbeute 21.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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