Use of miconazole and its derivatives as Tgr5 agonists
A technology of TGR5 and derivatives, applied in the field of biopathological diseases and diseases, miconazole, can solve the problems of strong toxic side effects and poor selectivity
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Embodiment 1
[0031] Example 1: 1-(2-(2,4-Dichlorophenyl)-2-((2,4-dichlorophenyl)methoxy)ethyl)-1H-1,2,4-tris azoles.
[0032]
[0033] The compound preparation method is as follows:
[0034] Step 1: Dissolve 2,2',3'-dichloroacetophenone (1 g, 4.47 mmol) in methanol, cool down to 0 °C in an ice bath, then add sodium borohydride (0.20 g, 5.37 mmol), gradually The reaction was raised to room temperature for 6 h, and the reaction was completed by TLC. 5 mL of saturated ammonium chloride solution was added to quench the reaction, concentrated under reduced pressure to remove methanol, the concentrated solution was extracted with ethyl acetate, dried over anhydrous sodium sulfate, and the concentrated reduction product was 0.91 g. Yield 90.1%.
[0035] The second step: The first step reduction product (1.0g, 4.43mmol) was dissolved in 20mL DMF, then 1,2,4-triazole (0.37g, 5.32mmol) and potassium hydroxide (0.50g, 8.87mmol) were added ), the temperature was raised to 60 °C for 6 h, and the ...
Embodiment 2
[0038] Example 2: 1-(2-(2,4-Dichlorophenyl)-2-((2,4-dichlorophenyl)methoxy)ethyl)-1H-imidazole.
[0039]
[0040] 1 H NMR (400MHz, DMSO-d 6 )δ7.68(d,J=2.1Hz,1H),7.59(d,J=2.0Hz,1H),7.52-7.44(m,2H),7.43-7.32(m,3H),7.05(s,1H) ), 6.85(s, 1H), 5.08(dd, J=6.6, 4.2Hz, 1H), 4.50–4.37(m, 2H), 4.35–4.21(m, 2H).
Embodiment 3
[0041] Example 3: 1-(2-(2,4-Dichlorophenyl)-2-((2,4-dichlorophenyl)methoxy)ethyl)-1H-pyrazole.
[0042]
[0043] 1 H NMR (400MHz, DMSO-d 6 )δ7.66(d,J=10.1Hz,2H),7.53(d,J=6.4Hz,3H),7.44(s,1H),7.35(d,J=7.0Hz,1H),7.21(d, J=7.0Hz, 1H), 6.23(s, 1H), 5.21(m, 1H), 4.34(m, 4H).
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