N-(2-cyanophenyl)picolinamide

COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #595490
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #963292
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #1298056
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #1592102
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #1973955
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #2017432
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #2049469
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #2367769
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
COc1c(I)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #2447177
product
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04