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2-Acetamido-6-methylpyrazine oxidation

Acetamido-6-methyl-5-oxo-4,5-dihydro-2-pyrazinecarbonitrile 1-oxide 3-Acetamido-6-methyl-5-oxo-4,5-dihydro-2-pyrazinecarboxamide 2-Acetamidomethylpyrazine 2-Acetamido-5-methylpyrazine... [Pg.351]

Amino-2prepared from 2-amino-3-cyanopyrazine 1-oxide by reflux with acetic acid-acetic anhydride followed by ready deacetylation by refluxing in methanol (538), and in a similar manner 3-amino-2-ethoxycarbonyl-5-hydroxypyrazine has been prepared from 2-amino-3-ethoxycarbonylpyrazine 1 -oxide through 3-acetamido-2-ethoxycarbonyl-5 ydroxy-pyrazine (538), and 2-amino-3-carbamoyl-6-hydroxy-5-methylpyrazine from 2-amino-3-cyano-5-methylpyrazine 1-oxide (538). The preparation of 24 ydroxy-6-methoxycarbonylpyrazine (10) has been claimed from 3-methoxycarbonylpyrazine 1-oxide with acetic anhydride followed by hydrolysis (1057) [cf. Nov Cek et al. (839), who claim it to be the 5-isomer, and Foks (744)]. [Pg.162]

Amino-3-cyano-5-methylpyrazine 1,4-dioxide (91) refluxed for several minutes with acetic anhydride formed 3-acetamido-2-cyano-5-hydroxy-6-methylpyrazine 1-oxide (92) (24%) (532) and 2-acetoxymethyl-5-methylpyrazine 1,4-dioxide refluxed with acetic anhydride afforded a mixture of2,5-di(acetoxymethyl)pyrazine 1-oxide, with some 2,5-diacetoxymethylpyrazine and a monoxide of 2-acetoxy-methyl-5-methylpyrazine (625). 2-Formylpyrazine hydrate 1,4-dioxide with aqueous sodium hydroxide or bicarbonate at < 37° in an unusual reaction gave 3-carboxy-pyrazine 1-oxide mixed with 5 [Pg.188]

Aminopyrazine jV-oxides may rearrange and acetylate in the presence of acetic anhydride. Thus 2-amino-3with acetic anhydride and acetic acid at reflux for 2 hours gave 3.acetamido-2-carbamoyl-5-hydroxypyrazine (25), 2-amino-3[Pg.216]

Alkylpyrazines with other substituents have been oxidized to carboxylic acids as follows 2-acetamido-6-methylpyrazine was oxidized in aqueous magnesium sulfate with potassium permanganate to 2-acetamido-6aqueous potassium permanganate at room temperature to 2-carboxy-3-chloropyrazine, which was also obtained by oxidation of 2-chloro-3-methylpyrazine with selenium dioxide in boiling aqueous pyridine (947). Oxidations of 2-methoxy-3-methyl-... [Pg.250]


See other pages where 2-Acetamido-6-methylpyrazine oxidation is mentioned: [Pg.243]    [Pg.307]   
See also in sourсe #XX -- [ Pg.250 ]




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2- -3-methylpyrazine oxidation

2- Methylpyrazine 1-oxide

2-Acetamido-6-methylpyrazine

2-Methylpyrazine

3- Acetamido-2-cyano-5-hydroxy-6-methylpyrazine 1-oxide

Methylpyrazines

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