Succinic acid amide derivatives of methoxynaphthalene ring, its preparation method and use
A technology of succinic acid and compounds, applied in the field of uric acid transporter 1 inhibitors, can solve problems such as fulminant hepatitis, allopurinol liver and bone marrow toxicity, and allergies
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Embodiment 1
[0025] .
[0026] A. Compound IV-1 Synthesis
[0027] 3.46g (20mmol) compound II-1 and 2.64g (20mmol) of compound III Dissolve in 50mL of dry THF, stir under ice-water bath cooling, add 4.13g (20mmol) of dicyclohexylcarbodiimide (DCC) and 0.61g (5mmol) of 4-dimethylaminopyridine (DMAP), and then stir at room temperature , until the TLC detection reaction was complete (within 12h). The reaction mixture was poured into 300 mL of ice water, stirred, using 100 mL × 3 CH 2 Cl 2 Extract, combine the extract phases, successively wash with 100mL of 1% dilute hydrochloric acid and 100mL of 5% brine, and dry 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 , white solid, ESI-MS, m / z =310([M+Na] + ).
[0028] B. Compound V-1 Synthesis
[0029] compound IV-1 4. Dissolve 30g (15mmol) in 30mL...
Embodiment 2-9
[0034] Referring to the operation steps of Example 1, the compounds listed in the following table were prepared.
[0035]
[0036]
Embodiment 10
[0038] The compounds of the present invention and related compounds inhibit IC of URAT1 50 The values are determined in a similar manner as described in the literature (Example 12 in US2014 / 0005136). The results are listed below.
[0039] Construction of a cell line stably expressing the humanized URAT1 transporter: The humanized URAT1 gene (SLC22A112) was subcloned from the plasmid pCMV6-XL-5 (Origene) into the eukaryotic expression plasmid pCMV6 / neo (Origene). Gene sequencing confirmed that the humanized URAT1 was consistent with the information recorded in the gene bank (NM_144585.2). HEK293 human embryonic kidney cells (ATCC#CRL-1573) were cultured in EMEM tissue culture medium under 5% CO 2 and 95% air atmosphere. pCMV6 / Neo / URAT1 was transfected onto HEK293 cells using L2000 type transfection reagent (Invitrogene). After 24 hours, the transfected cells were divided into tissue culture dishes with a diameter of 10 cm, continued to grow for one day, and then the mediu...
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