5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ylamine

NC(=O)c1ccc(-c2c[nH]c3ncc(-c4ccc(N)nc4)cc23)cc1
Reaction #172202
4-(5-(6-aminopyridin-3-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCc1cc(C)[nH]c(=O)c1CNC(=O)c1cc(-c2ccc(N)nc2)cc2c1cnn2C(C)C
Reaction #172615
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(-c2ccc(C(F)(F)F)c(C)c2)nc(-n2cnc(-c3ccc(N)nc3)c2)n1
Reaction #176756
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(-c2cccc(-c3cc(-c4ccc(Cl)cc4)cc(C(F)(F)F)n3)c2)cn1
Reaction #185193
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(-c2ccc(Cl)cc2)cc(-n2cnc(-c3ccc(N)nc3)c2)n1
Reaction #187353
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)N1CCN(Cc2cc3nc(-c4ccc(N)nc4)nc(N4CCOCC4)c3o2)CC1
Reaction #194640
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(-c2cn(-c3cc(-c4ccc(C(F)(F)F)cc4)cc(C4CC4)n3)cn2)cn1
Reaction #196351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)C(=O)N1CCN(Cc2cc3nc(-c4ccc(N)nc4)nc(N4CCOCC4)c3s2)CC1
Reaction #207507
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(-c2cn(-c3nc(-c4ccc(C(F)(F)F)c(F)c4)cc(C(F)(F)F)n3)cn2)cn1
Reaction #226196
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(F)cc1Oc1ccc(N)nc1
Reaction #228286
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(-c2ccc(C(F)(F)F)cc2)nc(-n2cc(-c3ccc(N)nc3)nc2C)n1
Reaction #231886
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1c(C(C)(C)O)nc2c(N3CCOCC3)nc(-c3ccc(N)nc3)nc21
Reaction #237338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(-c2ccc(Cl)c(Cl)c2)nc(-n2cnc(-c3ccc(N)nc3)c2)n1
Reaction #241366
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1ccc(-c2cn(-c3nc(-c4ccc(C(F)(F)F)cc4)cc(C(F)(F)F)n3)cn2)cn1
Reaction #260469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(-c2ccc(Cl)c(Cl)c2)cc(-c2cccc(-c3ccc(N)nc3)c2)n1
Reaction #265769
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1ccc(-c2cccc(-c3nc(-c4ccc(C(F)(F)F)cc4)cc(C(F)F)n3)c2)cn1
Reaction #272634
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(CO)c1ccc(C(=O)Nc2nc3ccc(-c4ccc(N)nc4)nc3s2)cc1
Reaction #274393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)c1cc(-c2ccc(C(F)(F)F)cc2)nc(-n2cnc(-c3ccc(N)nc3)c2)n1
Reaction #275365
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1ccc(-c2cc(Cl)nc(N3CCOCC3)n2)cn1
Reaction #284694
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(-c2ccc(Cl)cc2)nc(-c2ccnc(-c3ccc(N)nc3)c2)n1
Reaction #285069
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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