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Acylaminopyrazines deacylation

Acylaminopyrazines have been deacylated by hydrolysis in acid, or alkali, by methanolysis, or by hydrazinolysis (in propan-2-ol) under a variety of conditions to give the corresponding amino compound unless otherwise specified in the following examples 2-acetamido-3-acetoxymethylpyrazine (28) (dilute acetic acid at reflux for 6h) (1075) 2-acetamido-5-chloro-3-amidinocarbamoylpyrazine (5% hydrochloric acid-acetic acid at 100°) (150) 2-acetamido-3-A(-(benzimidoyl)-carbamoyl-5-chloropyrazine (5% hydrochloric acid at room temperature) (150) ... [Pg.217]

See other pages where Acylaminopyrazines deacylation is mentioned: [Pg.267]    [Pg.217]    [Pg.267]   
See also in sourсe #XX -- [ Pg.194 , Pg.210 , Pg.247 , Pg.267 ]

See also in sourсe #XX -- [ Pg.194 , Pg.210 , Pg.247 , Pg.267 ]



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Acylaminopyrazines

Deacylation

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