Compounds containing hydrazide structure, preparation method and application of compounds
The technology of a compound, hydrazine hydrate, is applied in organic chemistry, drug combination, nervous system diseases, etc., and can solve problems such as limited applications
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Embodiment 1
[0022] The synthesis of embodiment 1 compound I-1
[0023]
[0024] Step 1. Synthesis of Compound VI-1
[0025] Compound II (1.32g, 20mmol) was dissolved in 20mL DMSO, stirred at room temperature, KOH solid (2.24g, 40mmol) was added, and stirred at room temperature for 1 hour. Further MeI (III-1, 2.84 g, 20 mmol) was added, and stirring was continued overnight at room temperature. Then tert-butyl bromoacetate V-1 (3.90 g, 20 mmol) was added, and the stirring was continued for 12 hours. TLC detection found that the reaction was complete.
[0026] The reaction mixture was carefully poured into 200mL ice water, stirred, and washed with 50mL×3CH 2 Cl 2 After extraction, the extract phases were combined, washed with 100 mL of 5% brine, and dried over anhydrous sodium sulfate. The desiccant was removed by suction filtration, the filtrate was evaporated to dryness on a rotary evaporator, and the residue was purified by silica gel column chromatography to obtain compound VI-I,...
Embodiment 2
[0033] The synthesis of embodiment 2 compound 1-2
[0034]
[0035] Step 1. Synthesis of compound VI-2
[0036]Compound II (1.32g, 20mmol) was dissolved in 20mL DMSO, stirred at room temperature, KOH solid (2.24g, 40mmol) was added, and stirred at room temperature for 1 hour. Further MeI (III-1, 2.84 g, 20 mmol) was added, and stirring was continued overnight at room temperature. Then add 20mmol V-2 again, continue stirring for 12 hours, TLC detects that the reaction is complete. The reaction mixture was carefully poured into 200mL ice water, stirred, and washed with 50mL×3CH 2 Cl 2 After extraction, the extract phases were combined, washed with 100 mL of 5% brine, and dried over anhydrous sodium sulfate. The desiccant was removed by suction filtration, the filtrate was evaporated to dryness on a rotary evaporator, and the residue was purified by silica gel column chromatography to obtain compound VI-2. ESI-MS, m / z=271 ([M+H] + ).
[0037] Step 2. Synthesis of Comp...
Embodiment 3-4
[0042] With reference to the method of embodiment 1,2, synthesized following compound:
[0043]
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