Semicarbazone derivatives and application thereof
A technology of alkyl and compound, applied in the field of medicine, can solve problems such as toxic and side effects
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Embodiment 1
[0317] Example 1: (E)-N 1 -[2-(6-(4-Methylpiperidinyl)methylbenzo[d]thiazolyl)]-N 4 Preparation of -(2,4-dimethoxybenzaldehyde)semicarbazone
[0318] The preparation of step A N-(4-nitrobenzyl) diethylamine (1)
[0319] Add p-nitrobenzyl bromide (10.8g, 0.05mol) to 50mL of acetonitrile, add 10 times the amount of diethylamine, react at room temperature for 3h, add water to the reaction system, extract with dichloromethane three times, and dry the dichloromethane layer , evaporated to dryness to give 9.4g yellow liquid, yield: 90%, MS [MH + ] (m / z): 209.3.
[0320] Preparation of step B 4-(diethylaminomethyl)aniline (2)
[0321] Add intermediate 1 (10.4g, 0.05mol) to 100mL ethanol, raise the temperature to 70°C, add ferric chloride (2.8g, 0.001mol) and activated carbon (0.18g, 0.015mol), keep at 70°C, drop Add hydrazine hydrate (25g, 0.5mol), drop it, reflux for 5h, suction filter while it is hot, concentrate the ethanol solution, add water, extract three times with dichlo...
Embodiment 2
[0332] Example 2(E)-N 1 -[2-(6-(Diethylamino)methylbenzo[d]thiazolyl)]-N 4 -(4-Methoxybenzaldehyde)semicarbazone
[0333] ESI-MS [M+H] (m / z): 412.2;
Embodiment 3
[0334] Example 3(E)-N 1 -[2-(6-(Diethylamino)methylbenzo[d]thiazolyl)]-N 4 -(3-bromo-4-hydroxybenzaldehyde)semicarbazone
[0335] ESI-MS [M+H] (m / z): 476.1;
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