3- Acetamido-2-ethoxycarbonyl-5-hydroxypyrazine

Acetoxylative deoxygenations are as follows. 3-Methoxycarbonylpyrazine 1-oxide refluxed with acetic anhydride for 30 hours gave 2-acetoxy-6-methoxy-carbonylpyrazine (838), but Novdcek et al. (839) claim that the product (prepared with acetic anhydride at 160°) after hydrolysis with water was 2-hydroxy-5( )-methoxycarbonylpyrazine and 2-amino-3-ethoxycarbonylpyrazine 1-oxide refluxed with acetic acid-acetic anhydride gave 3-acetamido-2-ethoxycarbonyl-5-hydroxypyrazine (538). 

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)]. 

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]

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See also in sourсe #XX -- [ , , ]

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