Nitro containing and halogen benzene substituted 1H-tetrazole-1-acetic acid structure, and preparation method and use thereof
A compound and substituent technology, applied in the field of urate transporter 1 inhibitors, can solve the problems of allopurinol liver and bone marrow toxicity, allergy, fulminant hepatitis, etc.
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Embodiment 1
[0025] The synthesis of embodiment 1 compound I-1
[0026]
[0027] A. Synthesis of Compound IV-1
[0028] 3.76g (20mmol) of compound II-1 and 2.96g (20mmol) of compound III-1 were dissolved in 40mL of dry DMF, stirred, added 3.32g (20mmol) of potassium iodide and 6.91g (50mmol) of potassium carbonate, in a nitrogen atmosphere 100 React at °C until the reaction is complete (TLC tracking, generally 5h). After the reaction mixture was cooled, it was poured into 300 mL of ice water, stirred, and 100 mL × 3 CH 2 Cl 2 After extraction, the extract phases were combined, washed with 100 mL of 5% 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=278 ([M+Na] + ).
[0029] B. Synthesis of Compound VI-1
[0030] 3.06g (12mmol) of compound IV-1 and 1.76g (12m...
Embodiment 2-10
[0036] Referring to the operation steps of Example 1, the compounds listed in the following table were prepared.
[0037]
[0038]
[0039]
Embodiment 11
[0041] 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).
[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 cultured in 95% air atmosphere. pCMV6 / Neo / URAT1 was transfected onto HEK293 cells using L2000 type transfection agent (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 medium was replaced with f...
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