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Part – B Studies on isatin derivatives…..<br />

Fig. B.1.17<br />

Pandeya et. al. 248 synthesized Mannich bases of norfloxacin by<br />

reacting them with formaldehyde and several isatin derivatives. The starting<br />

materials 3-[4-sulfadiazinimino] isatin, 3-[4(-sulfadoximino] isatin and 3-[4'amino,<br />

5'-(3'', 4'', 5''-trimethoxybenzyl)pyrimidin-2'-yl]imino isatin and their 5substituted<br />

derivatives were prepared by reacting isatin and its derivatives<br />

with sulfadiazine, sulfadoxine and trimethoprim in the presence of glacial<br />

acetic acid. Mannich bases of norfloxacin were prepared by condensing the<br />

active hydrogen atom of isatin and the secondary amino function (piperazino<br />

moiety) of norfloxacin. (Fig. B.1.18)<br />

Fig. B.1.18<br />

Korepin et. al. 249 reported Mannich reactions of amino alchohols 3aminopropan-1-ol<br />

or 2-aminoethanol with formaldehyde and C-H or N-H acids<br />

gave N-substituted tetrahydro-1, 3-oxazines or oxazolidines. Thus, reaction<br />

Department of Chemistry, <strong>Saurashtra</strong> <strong>University</strong>, Rajkot-360 005 125

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