GPR119 agonist containing cyclopropyl hydrazide and halogenated benzene structures and application thereof
A halogen and substituent technology, applied in the field of GPR119 agonists, can solve the problems of decreased insulin secretion, unclear exact reasons, and decreased GIP activity
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Embodiment 1
[0028] The synthesis of embodiment 1 compound I-1
[0029]
[0030] A. Synthesis of Compound IV-1
[0031] Compound II-1 (1.08g, 10mmol) and compound III (1.95g, 10mmol) were dissolved in 20mL dry DMF, stirred at room temperature, solid potassium carbonate (4.15g, 30mmol) and 0.5g KI were added, and then heated at 80°C Stirring was continued until the reaction was complete (about 5 hours). The reaction mixture was poured into 150 mL ice water with 50 mL × 3 CH 2 Cl 2 After extraction, the extract phases were combined, washed with 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 obtained residue was purified by column chromatography to obtain compound IV-1, a white solid, ESI-MS, m / z=223 ([M+H] + ).
[0032] B. Synthesis of Compound V-1
[0033] Compound IV-1 (1.55g, 7mmol) was dissolved in 15mL of absolute ethanol, stirred at room temperature, 1mL of...
Embodiment 2-4
[0037] Referring to the method of Example 1, the compounds listed in the following table were synthesized.
[0038]
Embodiment 5
[0039] The synthesis of embodiment 5 reference compound D-1
[0040] In order to further illustrate the beneficial effect of the compound of the present invention, the applicant has recorded the compound D-1 and pharmacological data that the applicant has studied but not yet published.
[0041]
[0042] A. Synthesis of Compound IV-1
[0043] Compound II-1 (0.68g, 10mmol) and compound III (1.95g, 10mmol) were dissolved in 20mL dry DMF, stirred at room temperature, solid potassium carbonate (4.15g, 30mmol) and 0.5g KI were added, and then heated at 80°C Stirring was continued until the reaction was complete (about 5 hours). The reaction mixture was poured into 150 mL of ice water, extracted with 50 mL×3 of CH2Cl2, the combined extracts were washed with 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 obtained residue was purified by column chromatography ...
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