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

NaOH and R 2 CH2CH2Cl.HCl gave 61-73 % (3) (R 2 = morpholino, piperidino,<br />

pyrrolidino). (Fig. B.1.12)<br />

Collino and Volpe 242 prepared Mannich bases from benzimidazoles,<br />

benzotriazoles, indolones, or benzoxazolones and N-phenylpiperazine, 4anilinopiperidine,<br />

4-benzylpiperidine, or N-bezylpiperazine.<br />

R 1<br />

R 1<br />

N<br />

R<br />

X<br />

O<br />

N<br />

H<br />

I<br />

N<br />

N<br />

N<br />

S CH 2CH 2R 2<br />

The same authors 243 further prepared Mannich bases of N<br />

heterocycles or aromatic amines with trimethylenedipiperidine, dipiperidine,<br />

and hydroxyethyldipiperidine as well as the isatin derivatives (where, n = 6, 7).<br />

(Fig. B.1.13)<br />

N<br />

1<br />

O<br />

3<br />

O<br />

O<br />

O<br />

N<br />

CO(CH 2 )nCO<br />

I<br />

R 1<br />

244<br />

Jancevska-Nikolovska converted the hexylbenzene into 4hexylaniline<br />

which underwent cyclization reactions to give acridines,<br />

benzacridines, isatins, carbazoles, indoles, benzindoles, quinolines, and<br />

benzoquinolines. (all substituted with the hexyl group) Further they carried out<br />

Mannich reaction to give N-substituted derivatives. (Fig. B.1.14)<br />

Department of Chemistry, <strong>Saurashtra</strong> <strong>University</strong>, Rajkot-360 005 123<br />

2<br />

Fig. B.1.12<br />

Fig. B.1.13<br />

N<br />

H<br />

N NH<br />

N<br />

III<br />

S<br />

II

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