An 123 Reaktionen beteiligt

134

Cc1cccnc1N[C@@H]1CCCN(C(=O)OC(C)(C)C)C1
Reaction #656
Ausbeute 69.8%750 AstraZeneca ELN dataset
Cc1cccnc1N[C@@H]1CCCN(C(=O)OC(C)(C)C)C1
Reaction #657
Ausbeute 82.4%750 AstraZeneca ELN dataset
Cc1cccnc1NC1CCCCC1
Reaction #713
Ausbeute 61.8%750 AstraZeneca ELN dataset
COc1cc(-c2nc3ccccc3o2)ccc1-c1ccc(C)cn1
Reaction #7883
2-[3-methoxy-4-(5-methylpyridin-2-yl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccnc1-c1cccc(C(=O)OC(C)(C)C)c1
Reaction #85462
tert-butyl-3-(3-methylpyridin-2-yl)benzoate
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-c2cnn(C)c2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncccc2C)c1
Reaction #89301
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cccnc1-c1cccc(C(=O)OC(C)(C)C)c1
Reaction #169521
tert-butyl-3-(3-methylpyridin-2-yl)benzoate
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cccnc1N1CC(C(=O)OC(C)(C)C)N(C)C1=O
Reaction #192740
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CN(Cc2ccc(OC)cc2)c2ncc(-c3nc(N4CCOCC4)nc4c3CCN4c3ncccc3C)cn2)cc1
Reaction #212030
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccnc1C(O)c1cc(C)c(C)o1
Reaction #266857
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cccnc1C(C#N)c1ccc(F)cc1
Reaction #269094
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cccnc1C(=O)c1cn(-c2cccc(-c3ccccc3OC(F)(F)F)c2)cn1
Reaction #285986
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cccnc1C(=O)c1cn(-c2cccc(-c3ccccc3Cl)c2)cn1
Reaction #296489
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cccnc1C(O)c1cc(C)c(C)o1
Reaction #316230
(4,5-dimethylfuran-2-yl)-(3-methyl-pyridin-2-yl)-methanol
Ausbeute 66.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1cccnc1-c1cc(C)c(Br)c(C)c1
Reaction #324856
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cccnc1C(=O)c1cn(-c2cccc(-c3cccnc3F)c2)cn1
Reaction #387847
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1c(F)cccc1-c1cccc(-n2cnc(C(=O)c3ncccc3C)c2)c1
Reaction #393036
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cccnc1NN
Reaction #396689
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cccnc1N1CCNCC1
Reaction #398216
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cccnc1NC(C)(C)C
Reaction #422026
N-tert-Butyl-3-methylpyridin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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