Reaction of aromatic N-oxides with dipolarophiles. VIII. Carbamation products of 2-anilinopyridine derivatives.
نویسندگان
چکیده
منابع مشابه
REACTIVITY OF N-SUBSTITUTED p-BENZO AND p-NAPHTHOQUINONEIMINE N-OXIDES TOWARD DIPOLAROPHILES
The dipolar cycloaddition reactivity of N-(1-naphthy1)-1,4- benzoquinoneimine N-oxide and N-phenyl-1,4- naphthoquinoneimine Noxide are investigated, The latter gives the expected adducts with common dipolarophiles such as acrylonitryle, methyl methacrylate, dimethylacetylene dicarboxylate and N-phenylmaleimide. The reactivity of the former nitrone is found to be minimal. It undergoes, how...
متن کاملReaction of benzoylpyruvate with a mixture of aromatic aldehydes and 5-amino-1,3,4-thiadizole-2-thiol
Reactions of benzoylpyruvate with a mixture of aromatic aldehydes and 5-amino-1,3,4-thiadizole-2-thiol in a 1:1:1 molar ratio, afforded 5-(5-aryl-4-benzoyl-3-hydroxy-2-oxo-2,5-dihydro-1H-pyrrol-1-yl)-1,3,4-thiadizole-2-thiols (3a-c). The structure of the resulted products was confirmed by determination of the melting point and spectrophotometric techniques such as IR and 1H-NMR spectroscopy.
متن کاملMutagenicity of derivatives of the oncogenic purine N-oxides.
Acetoxy esters of purine W-oxides inactivate and induce mutations in Bacillus jwà ̈n/Ã1-transforming DNA. The es ters were the chemical models available for the sulfate es ters believed to be formed in vivo. When metabolic suscep tibilities were taken into consideration, there is a reasonable correlation between the mutagenicity of various acetoxy es ters and the oncogenicity of the parent W-oxi...
متن کاملPreparation of sterically congested 1,3,4-oxadiazole derivatives from N-isocyaniminotriphenylphosphorane, aromatic acids, cyclopentanone and primary amines
Reactions of N-isocyaniminotriphenylphosphorane with cyclopentanone have been studied in the presence of aromatic carboxylic acids and primary amines, proceeds smoothly at room temperature under neutral conditions to afford sterically congested 1,3,4-oxadiazole derivatives by an intramolecular Aza-Wittig cyclization in CH2Cl2 in excellent yields. The structures of the products were deduced from...
متن کاملPurine N-oxides. XVI. Oncogenic derivatives of xanthine and guanine.
The oxidation of guanine to an N-oxide and its hydrolysis to a xanthine N-oxide are rejorted. The s.c. administration of the xanthine N-oxide to rats for 6 months resulted in development of a variety of tumors. There were 1 liposarcoma, 3 fibrosarcomas, 1 nmmmary adenocarcinoma, 3 fibrohlastic tumors, 2 rhabdomyosarcomas, and 1 epideiinoid carcinoma at the site of injection and elsewhere in 11 ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Chemical and Pharmaceutical Bulletin
سال: 1985
ISSN: 0009-2363,1347-5223
DOI: 10.1248/cpb.33.1869