A kind of diketone derivative and its preparation method and application
A technology of derivatives and diketones, applied in the field of diketone derivatives and their preparation, can solve problems such as affecting the polymerization process of tau protein, and achieve the effects of protecting nerve cells, treating Alzheimer's disease, and having strong stabilizing effects.
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Embodiment 1
[0032] Synthesis of 5-bromo-2-(2,6-diisopropyl-phenyl)-isoindole-1,3-dione 1a
[0033] Weigh 4-bromophthalic anhydride (0.67mmol, 1eq) and compound 2,6-diisopropylaniline (0.80mmol, 1.2eq) in a 25mL round bottom bottle, dissolve it in acetonitrile (3mL) After that, add DPPOx (1.34mmol, 2eq) prepared by reference (Tetrahedron, 1982,39 (20): 3253), Et 3 N (0.18mL, 1.29mmol, 1.9eq), the reaction continued for 2.5h under the condition of reflux, and the reaction was monitored by TLC until the raw materials disappeared completely, the reaction solution was spin-dried, and the reactant was redissolved in ethyl acetate, respectively With HCl (30mL, 3M) and NaHCO 3 (30mL, 3M) washed with water and extracted. The extract was collected and dried, spin-dried, and purified by column chromatography to obtain product 1a, a white solid, melting point: 165° C., yield 92%.
[0034] 1 H NMR (400MHz, CDCl 3 )δ8.11(d, J=3.8Hz, 1H), 7.96(dd, J=7.9, 1.4Hz, 1H), 7.84(d, J=7.9Hz, 1H), 7.46(t, J=...
Embodiment 2
[0036]Synthesis of 5-bromo-2-(3,4,5-trimethoxy-phenyl)-isoindole-1,3-dione 1b
[0037] Compound 4-bromophthalic anhydride (0.67mmol) and compound 3,4,5-trimethoxyaniline (0.80mmol) were isolated according to the operation process of Example 1 to obtain compound 1b, a white solid, melting point: 200°C,
[0038] Yield 88%.
[0039] 1 H NMR (400MHz, CDCl 3 )δ8.09(d, J=0.8Hz, 1H), 7.94(dd, J=7.9, 1.3Hz, 1H), 7.82(d, J=7.9Hz, 1H), 6.63(s, 2H), 3.89( s,3H),3.88(s,6H); ESI-MS m / z:392.1[M+H] + .
Embodiment 3
[0041] Synthesis of 6-(2,6-diisopropyl-phenyl)pyrrolo(3,4-b)pyridine-5,7-dione 1c
[0042] Compound 2,3-pyridinedicarboxylic acid anhydride (0.67mmol) and compound 2,6-diisopropylaniline (0.80mmol) were separated according to the operation process of Example 1 to obtain compound 1c, a white solid, melting point: 170°C, and obtained rate 56%.
[0043] 1 H NMR (400MHz, DMSO) δ9.11 (dd, J = 5.0, 1.4Hz, 1H), 8.46 (dd, J = 7.7, 1.4Hz, 1H), 7.92 (dd, J = 7.7Hz, 1H), 7.54 (t, J=7.7Hz, 1H), 7.37(d, J=7.7Hz, 2H), 2.73(hept, J=6.8Hz, 2H), 1.07(d, J=7.7Hz, 12H); ESI-MS m / z:309.2[M+H] + .
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