Succinic acid amide derivatives containing phenylnaphthalene rings as well as preparation method and application thereof
A technology of alkyl and compounds, applied in the field of uric acid transporter 1 inhibitors, can solve problems such as allopurinol liver and bone marrow toxicity, fulminant hepatitis, and allergic reactions
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Embodiment 1
[0029] .
[0030] A. Compounds IV-1 Synthesis
[0031] 5.06g (20 mmol) compound II-1 and 2.64 g (20 mmol) of compound III Dissolve in 50 mL of dry THF, stir under ice-water bath cooling, add 4.13 g (20 mmol) of dicyclohexylcarbodiimide (DCC) and 0.61 g (5 mmol) of 4-dimethylaminopyridine (DMAP), and then Stir at room temperature until the reaction is complete (within 12 h) as detected by TLC. 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 100 mL of 1% dilute hydrochloric acid and 100 mL 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 = 390([M+Na] + ).
[0032] B. Compounds V-1 Synthesis
[0033] compound IV-1 Dissolve 5.50 ...
Embodiment 2-16
[0038] Referring to the operation steps of Example 1, the compounds listed in the following table were prepared.
[0039]
Embodiment 17
[0041] The compounds of the present invention and related compounds inhibit IC of URAT1 50The values are determined in a similar manner as described in the literature (Example 12 in US2014 / 0005136). The results are listed below.
[0042] 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 10 cm diameter tissue culture dishes and grown for another day, after which the medium was replac...
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