2,6-dichloropyridine

N#Cc1ccc(Cl)cc1Nc1cccc(Cl)n1
Reaction #519
Ausbeute 93.5%750 AstraZeneca ELN dataset
Clc1cccc(Nc2ccccc2)n1
Reaction #734
Ausbeute 53.0%750 AstraZeneca ELN dataset
Clc1ccc(C23CCCN2CCC3)c(Cl)n1
Reaction #3391
oil
Ausbeute 17.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1cccc(-n2c(/C=C/c3ccccc3)nc3ccccc32)n1
Reaction #79153
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Clc1cccc(OCc2cccs2)n1
Reaction #83396
2-chloro-6-(2-thienylmethyloxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Clc1cccc(OCc2ccsc2)n1
Reaction #83398
2-chloro-6-(3-thienylmethyloxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cccc(-c2cccc(Cl)n2)c1
Reaction #158256
2-chloro-6-(3-methoxyphenyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[C@H](Nc1cccc(Cl)n1)c1ccc(F)cc1
Reaction #163108
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(-c2cccc(Cl)n2)cc1
Reaction #186810
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1cccc(OCc2ccccc2)n1
Reaction #191171
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1cccc(Nc2nccs2)n1
Reaction #194785
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[O-][n+]1c(Cl)cccc1Cl
Reaction #201294
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1cccc(Oc2cccc(Cl)n2)c1
Reaction #201964
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1cccc(OC2CCN(CC3CC3)CC2)n1
Reaction #209543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #216728
2,3,5,6-Tetrachloropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
Cc1ccc(S(=O)(=O)N(C)c2cccc(Cl)n2)cc1
Reaction #224026
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Fc1ccccc1Sc1cccc(Cl)n1
Reaction #239889
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(N)COc1cccc(Cl)n1
Reaction #264509
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CCC(C(Oc2cccc(Cl)n2)c2ccc(Br)cc2)CC1
Reaction #286000
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OC(c1ccccc1Cl)c1ccc(Cl)nc1Cl
Reaction #358256
(2-chloro-phenyl)-(2,6-dichloro-pyridin-3-yl)-methanol
Ausbeute 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
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