amide

N#Cc1cc(Cl)ccn1
Reaction #43366
title compound
Yield 87.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #75962
oil
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
NC(=O)c1cc(Oc2cccc(N)c2)ccn1
Reaction #165525
3-(2-carbamoyl-4-pyridyloxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=O)c1cc(Oc2ccc(N)cc2)ccn1
Reaction #165528
4-(2-carbamoyl-4-pyridyloxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=O)c1cc(Oc2ccc(N)cc2)ccn1
Reaction #165543
4-(2-carbamoyl-4-pyridyloxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=O)c1cc(Oc2cccc(N)c2)ccn1
Reaction #165545
3-(2-carbamoyl-4-pyridyloxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=O)c1cc(Oc2c(F)cc(N)cc2F)ccn1
Reaction #188804
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1cc(Oc2cc(F)c(N)cc2F)ccn1
Reaction #194994
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1cc(Oc2ccc(N)c(F)c2F)ccn1
Reaction #248702
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)c1cc(Oc2ccc(N)c(F)c2)ccn1
Reaction #266422
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)c1cc(Oc2ccc(N)cc2Cl)ccn1
Reaction #283465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)c1cc(Oc2cccc(CO)c2)ccn1
Reaction #294272
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)c1cc(Oc2c(F)cc(N)cc2F)ccn1
Reaction #300473
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)c1cc(Oc2cc(F)c(N)cc2F)ccn1
Reaction #384249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CNC(=O)c1cc(Oc2ccc(-c3nnc(Nc4ccc(OC(F)(F)F)cc4)[nH]3)cc2)ccn1.O=C(O)C(F)(F)F
Reaction #474624
TFA
Yield 40.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CNC(=O)c1cc(Oc2ccc(Nc3nnc(-c4ccc(OC(F)(F)F)cc4)[nH]3)cc2)ccn1.O=C(O)C(F)(F)F
Reaction #474634
TFA
Yield 27.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CNC(=O)c1cc(Oc2cccc(-c3nnc(Nc4ccc(Cl)c(C(F)(F)F)c4)[nH]3)c2)ccn1.O=C(O)C(F)(F)F
Reaction #474636
TFA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CNC(=O)c1cc(Oc2ccc(-c3nnc(Nc4ccc(Cl)c(C(F)(F)F)c4)o3)cc2)ccn1.O=C(O)C(F)(F)F
Reaction #474645
title product
Yield 79.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Nc1ccc(Oc2ccncc2)cc1F
Reaction #475678
title compound
Yield 90.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Nc1ccc(Oc2ccncc2)cc1F
Reaction #475679
title compound
Yield 91.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
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