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2,5- Dimethyl-3-isopentyl-6- pyrazines

In the pyrazine series, the Mannich reaction was applied first to 2,5-dimethyl-pyrazine by Linder and Spoerri (715). Of the amines tried, positive reactions were obtained only with dime thy lamine, piperidine, and morpholine, and it was found that one, or more usually two, of the hydrogen atoms of each of the methyl groups could be substituted. Thus 2,5-dimethylpyrazine, dimethylamine hydrochloride, and formalin in refluxing isopentyl alcohol gave 2,5-bis[bis(dimethylaminomethyl)-methyl]pyrazine and 2,5-bis(j3-dimethylaminoethyl)pyrazine. Reaction of 2-methyl-pyrazine with formalin and diethylamine hydrochloride gave 2- 3-diethylamino-ethylpyrazine (716) similarly dimethylamine hydrochloride gave 2-dimethyl-aminoethylpyrazine (17) and some 2-[bis(dimethylaminomethyl)]methylpyrazine (18) (657). [Pg.83]


See other pages where 2,5- Dimethyl-3-isopentyl-6- pyrazines is mentioned: [Pg.197]    [Pg.5]   
See also in sourсe #XX -- [ Pg.5 , Pg.226 , Pg.245 , Pg.266 ]




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2, 5-Dimethyl pyrazine

Isopentyl

Isopentyl)-pyrazines

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