O-(2,4-dinitrophenyl)hydroxylamine

Cc1cc2c[n+](N)ccc2o1
Reaction #197606
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(-n2c(=O)cc(C(F)(F)F)n(N)c2=O)ccc1C#N
Reaction #206803
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1ccc(C(=O)c2ccc(C#N)cc2)n1N
Reaction #237290
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCc1cc2c(Cl)cc(F)c(-n3c(=O)cc(C(F)(F)F)n(N)c3=O)c2o1
Reaction #252830
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)C(=O)Nc1nc2c(c(NC(=O)C(C)(C)C)n1)CC(=NOc1ccccc1)CC2
Reaction #298249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(N)C1=O
Reaction #299451
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C1(N)N=C(c2ccccc2Cl)c2cc(CC)sc2-n2c(C3CCCCC3)nnc21
Reaction #321228
ethyl(6-amino-4-(2-chlorophenyl)-9-cyclohexyl-2-ethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
C=C(Oc1cc(-n2c(=O)cc(C(F)(F)F)n(N)c2=O)c(F)cc1Cl)C(=O)OC
Reaction #370056
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=[N+]([O-])c1ccc([O-])c([N+](=O)[O-])c1
Reaction #370449
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CON=Cc1c(Cl)ccc(-n2c(=O)cc(C(F)(F)F)n(N)c2=O)c1F
Reaction #374552
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C1(N)N=C(c2ccccc2Cl)c2cc(CC)sc2-n2c(C3CCCCC3)nnc21
Reaction #393364
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cn(N)c2c(OC)c(F)c(F)cc2c1=O
Reaction #446075
ethyl 1-amino-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate
수율 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
CCc1cc2c(Cl)cc(F)c(-n3c(=O)cc(C(F)(F)F)n(N)c3=O)c2o1
Reaction #453498
desired product
수율 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Nn1c(C(F)(F)F)cc(=O)n(-c2cc(Oc3ncccc3[N+](=O)[O-])c(Cl)cc2F)c1=O
Reaction #467489
semi-solid
수율 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Nn1c(C(F)(F)F)cc(=O)n(-c2cc(Oc3ccccc3[N+](=O)[O-])c(Cl)cc2F)c1=O
Reaction #467491
solid
수율 43.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
—
Reaction #467494
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
—
Reaction #467496
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COc1cc(-n2c(=O)cc(C(F)(F)F)n(N)c2=O)ccc1C#N
Reaction #518102
desired product
수율 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
CCOC(=O)c1cn(N)c2nc(C)ccc2c1=O
Reaction #549874
ethyl 1-amino-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylate
수율 63.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_05
CC(C)(C)OC(=O)Nc1cc[n+](N)cc1.O=[N+]([O-])c1ccc([O-])c([N+](=O)[O-])c1
Reaction #600214
1-amino-4-(tert-butoxycarbonylamino)pyridinium 2,4-dinitrophenolate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
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