3-nitrobenzoyl chloride

O=C1CCC(N2C(=O)c3cccc(NC(=O)c4cccc([N+](=O)[O-])c4)c3C2=O)C(=O)N1
Reaction #10098
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(c1ccc(Br)cc1)c1cccc([N+](=O)[O-])c1
Reaction #64265
white crystals
Ausbeute 91.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1ccc(NC(=O)c2cccc([N+](=O)[O-])c2)c(C(N)=O)c1
Reaction #89908
5-Methoxy-2-(3-nitrobenzoyl)aminobenzamide
Ausbeute 133.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cc(Nc2cccc([N+](=O)[O-])c2)c(C(N)=O)cc1OC
Reaction #89915
4,5-dimethoxy-2-(3-nitrophenyl)aminobenzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COCCOc1cc(C(N)=O)c(Nc2cccc([N+](=O)[O-])c2)cc1OC
Reaction #89942
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1cccc([N+](=O)[O-])c1)c1cccc([N+](=O)[O-])c1
Reaction #93887
3,3'-Dinitrobenzanilide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
O=C(Nc1ccc(S(=O)(=O)[O-])c2cccc(O)c12)c1cccc([N+](=O)[O-])c1.[Na+]
Reaction #94605
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1cccc([N+](=O)[O-])c1
Reaction #95217
pure product
Ausbeute 69.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CNC1=NN(C(=O)c2cccc([N+](=O)[O-])c2)C(C)(C)S1
Reaction #96008
5,5-Dimethyl-2-methylamino-4-(3-nitrobenzoyl)-4,5-dihydro-1,3,4-thiadiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)C1CCN(C(=O)c2cccc(N)c2)CC1
Reaction #158513
3-[4-(ethoxycarbonyl)piperidinocarbonyl]aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NNC(=O)c1cccc([N+](=O)[O-])c1)c1cccc(Cl)c1
Reaction #158525
N′1-(3-chlorobenzoyl)-3-nitrobenzene-1-carbohydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C1CCN(C(=O)c2cccc(N)c2)CC1
Reaction #163623
3-[4-(ethoxycarbonyl)piperidinocarbonyl]aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NNC(=O)c1cccc([N+](=O)[O-])c1)c1cccc(Cl)c1
Reaction #163634
N′1-(3-chlorobenzoyl)-3-nitrobenzene-1-carbohydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1cccc([N+](=O)[O-])c1)N1CCOCC1
Reaction #185757
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(Cc1ccccc1)C(=O)c1cccc([N+](=O)[O-])c1
Reaction #188818
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4cccc([N+](=O)[O-])c4)c3C2=O)C(=O)N1
Reaction #189209
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(NC(=O)c2cccc([N+](=O)[O-])c2)cc1
Reaction #192104
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccccc1Oc1ccc(-c2nnnn2Cc2ccccc2)c(-c2nnnn2Cc2ccccc2)c1)c1cccc([N+](=O)[O-])c1
Reaction #193093
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C(=O)c2cccc([N+](=O)[O-])c2)cc1OC
Reaction #195928
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(c1ccccc1)n1cnc2ccc(NC(=O)c3cccc([N+](=O)[O-])c3)cc21
Reaction #199587
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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