(2-chloro-4-pyridinyl)methanol

CN(c1ccc(F)cc1)c1cc(CO)ccn1
Reaction #354
Выход 0.0%750 AstraZeneca ELN dataset
Fc1ccc(OCc2ccnc(Cl)c2)cc1
Reaction #43336
title compound
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cc(CBr)ccn1
Reaction #169636
4-(bromomethyl)-2-chloropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(CO)ccn1
Reaction #169643
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CS(=O)(=O)OCc1ccnc(Cl)c1
Reaction #188694
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1cc(CBr)ccn1
Reaction #274037
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Clc1cc(CBr)ccn1
Reaction #309414
4-bromomethyl-2-chloropyridine
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cl.ClCc1ccnc(Cl)c1
Reaction #366778
2-chloro-4-chloromethylpyridine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CNc1cc(CO)ccn1
Reaction #366853
4-hydroxymethyl-2-(methylamino)pyridine
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CN(C)c1cc(CO)ccn1
Reaction #366855
4-hydroxymethyl-2-(dimethylamino)pyridine
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
ClCc1ccnc(Cl)c1
Reaction #371585
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=Cc1ccnc(Cl)c1
Reaction #383639
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Clc1cc(COc2ccccc2)ccn1
Reaction #393204
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=Cc1ccnc(Cl)c1
Reaction #411225
2-chloropyridine-4-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=Cc1ccnc(Cl)c1
Reaction #411885
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=Cc1ccnc(Cl)c1
Reaction #431190
title compound
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=Cc1ccnc(Cl)c1
Reaction #449800
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CC(C)(C)[Si](C)(C)OCc1ccnc(Cl)c1
Reaction #494376
4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COc1cc(CO)ccn1
Reaction #513424
(2-Methoxy-pyridin-4-yl)-methanol
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Clc1cc(CBr)ccn1
Reaction #580416
4-bromomethyl-2-chloropyridine
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
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