4-chloro-3-nitropyridine

N#Cc1ccc(N2C=CC(N)=C([N+](=O)[O-])C2)cc1
Reaction #6451
N-(4-cyanophenyl)-4-amino-3-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=[N+]([O-])c1cnccc1NCCCO
Reaction #50772
4-(3-hydroxypropylamino)-3-nitropyridine
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=[N+]([O-])c1cnccc1F
Reaction #62547
4-fluoro-3-nitropyridine
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=C(O)c1cccc(-c2ccncc2[N+](=O)[O-])c1
Reaction #72270
3-(3-nitropyridin-4-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1cnccc1N1CCCCC1
Reaction #157009
3-nitro-4-(piperidin-1-yl)pyridine
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)NC1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157010
tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N[C@@H]1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157011
(R)-tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N[C@H]1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157012
(S)-tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)NCC1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157013
tert-butyl (1-(3-nitropyridin-4-yl)piperidin-3-yl)methylcarbamate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C)CCN(C)c1ccncc1[N+](=O)[O-]
Reaction #157017
N1,N1,N2-trimethyl-N2-(3-nitropyridin-4-yl)ethane-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)NC1CCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157018
tert-butyl 1-(3-nitropyridin-4-yl)pyrrolidin-3-ylcarbamate
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)NCCOc1ccncc1[N+](=O)[O-]
Reaction #157046
tert-butyl 2-(3-nitropyridin-4-yloxy)ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cnccc1C1=CCCCC1
Reaction #157056
4-cyclohexenyl-3-nitropyridine
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C(=O)O)CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157089
3-methyl-(3-nitropyridin-4-yl)piperidine-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cnccc1N1CCC[C@H](O)C1
Reaction #157095
(S)-1-(3-nitropyridin-4-yl)piperidin-3-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cnccc1N1CCC[C@@H](O)C1
Reaction #157096
(R)-1-(3-nitropyridin-4-yl)piperidin-3-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cnccc1N1CCCC(O)C1
Reaction #157097
(+/−)-1-(3-nitropyridin-4-yl)piperidin-3-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(O)CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157106
3-methyl-1-(3-nitropyridin-4-yl)piperidin-3-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(-c2ccncc2[N+](=O)[O-])cc(N)n1
Reaction #157151
6-methyl-3′-nitro-4,4′-bipyridin-2-amine
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N[C@H]1C[C@@H](F)CN(c2ccncc2[N+](=O)[O-])C1
Reaction #157165
titled compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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