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Chapter – 2 Microwave assisted simple and fast…..<br />

2.4.5 GENERAL PROCEDURE FOR THE PREPARATION OF DNJ-601 to<br />

DNJ-605<br />

0.01 mole of an appropriate side chain (SC-06 to SC-10) was charged<br />

into 250 ml erlenmeyer flask loosely covered with gravity funnel. 0.015 mole<br />

of anhydrous potassium carbonate was added followed by addition of 0.01<br />

mole of isatin into above flask. 1 ml of dimethylformamide was added in order<br />

to make slurry. The reaction mixture was irradiated under microwave<br />

irradiation into household microwave oven (LG MS-192 W) at 480 W for<br />

desired time. The progress and the completion of the reaction were checked<br />

by silica gel-G F254 thin layer chromatography using toluene : ethyl acetate (7 :<br />

3) as mobile phase. The reaction mixture was then taken into 50 ml water and<br />

it was extracted with ethyl acetate (30 ml X 3), the combined organic layer<br />

was washed using water (20 ml X 2). The organic layer was dried on<br />

anhydrous sodium sulphate and the solvent was removed under reduced<br />

pressure to acquire the product. (Physical data of the synthesized end<br />

products are summarized in the table 2.5.4)<br />

Code<br />

No.<br />

Substitution<br />

R1 & R2<br />

Reaction Time<br />

(min.) (at 480 W)<br />

% Yield<br />

DNJ-601 Piperidine 7.5 79<br />

DNJ-602 Morpholine 7.0 81<br />

DNJ-603 1-Methyl Piperazine 7.4 75<br />

DNJ-604 1-Ethyl Piperazine 7.5 80<br />

DNJ-605 1-Benzyl Piperazine 7.3 74<br />

Department of Chemistry, <strong>Saurashtra</strong> <strong>University</strong>, Rajkot – 360 005 83

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