2-Aminonicotinaldehyde

Fc1cccc(F)c1-c1ccc2cccnc2n1
Reaction #926
desired product
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1cnc2nc(-c3nccs3)ccc2c1
Reaction #927
desired product
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1cc2cccnc2nc1O
Reaction #75338
2-Hydroxy-3-cyano-1,8-naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1ncccc1C=NO
Reaction #165038
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Br.Nc1ncc(Br)cc1C=O
Reaction #170203
title compound
Ausbeute 165.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)C(=O)Nc1ncccc1C=O
Reaction #219399
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)(C)C(=O)Nc1ncccc1C=O
Reaction #219534
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
N#Cc1cccc2c1OC(c1cccnc1N)N2
Reaction #245545
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(O)c1cccnc1N
Reaction #310058
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1nc2ncccc2cc1O
Reaction #316082
2-methyl-[1,8]naphthyridin-3-ol
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Oc1cc2cccnc2nc1-c1ccccn1
Reaction #316213
2-pyridin-2-yl-[1,8]naphthyridin-3-ol
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Oc1cc2cccnc2nc1-c1ccccc1
Reaction #316215
2-phenyl-[1,8]naphthyridin-3-ol
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCc1nc2ncccc2cc1O
Reaction #316217
2-ethyl-[1,8]naphthyridin-3-ol
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)c1nc2ncccc2cc1O
Reaction #316225
2-tert-butyl-[1,8]naphthyridin-3-ol
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1ccc(-c2nc3ncccc3cc2O)cc1
Reaction #316228
2-p-toluyl-[1,8]naphthyridin-3-ol
Ausbeute 1.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Nc1ncc(I)cc1C=O
Reaction #390617
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C[C@@H](c1cccc(F)c1)N1CCCC(CCCc2ccc3cccnc3n2)C1=O
Reaction #409256
2-8
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOC(=O)C(C)N(CCCc1ccc2cccnc2n1)C(=O)OC(C)(C)C
Reaction #409264
4-7
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOC(=O)CN1C(=O)[C@@H](CCc2ccc3cccnc3n2)C[C@H]1C
Reaction #409699
11-10
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CC(C)(C)OC(=O)N1CCC(c2ccc3cccnc3n2)CC1
Reaction #438830
title compound
Ausbeute 24.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
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