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Acetone Iproniazid

Thus, condensation of isoniazide with acetone at the basic nitrogen gives the corresponding Shiff base (8). Catalytic reduction affords the antidepressant, iproniazid (9). Addition of the same basic nitrogen to methyl acrylate by Michael condensation leads to the 3-amino ester (10). This is converted to the amide, nialamide (11), on heating with benzylamine. [Pg.254]

Iproniazid phosphate [305-33-9] M 277.2, m 178-179". Crystd from water and acetone. [Pg.246]


See other pages where Acetone Iproniazid is mentioned: [Pg.2280]    [Pg.2280]   


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