Application of 16034-46-1,Some common heterocyclic compound, 16034-46-1, name is 1-Methyl-1H-pyrazole-5-carboxylic acid, molecular formula is C5H6N2O2, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.
DIPEA (1.05 mL, 6.35 mmol) was added to a stirred solution of Intermediate 1130 (500 mg, 2.12 mmol), 1-methyl-1H-pyrazole-5-carboxylic acid (269 mg, 2.12 mmol) andHATU (969 mg, 2.55 mmol) in anhydrous DMF (10 mL) under a nitrogen atmosphere.The mixture was stirred at 20C for 18 h, then quenched with saturated aqueous sodiumhydrogen carbonate solution (50 mL) and water (50 mL). The material was extracted with ethyl acetate (3 x 50 mL). The combined organic layers were washed with brine (2 x50 mL) and dried over sodium sulfate, then filtered and concentrated in vacuo. Theresidue was purified by flash column chromatography, using a gradient of ethyl acetate inheptane (0-100%), to afford the title compound (618 mg, 99%) as a yellow-orange oil. DH5 (500 MHz, DMSO-d6) 8.60 (d,J8.3 Hz, 1H), 7.46 (d,J2.1 Hz, 1H), 7.01 (d,J2.1 Hz,1H), 4.37 (t, J8.1 Hz, 1H), 4.01 (s, 3H), 3.66 (s, 3H), 2.22-2.08 (m, 1H), 1.80-1.38 (m,13H), 1.37-1.29 (m, 1H). HPLC-MS (method 5): MH+ m/z 308, RT 1.87 minutes.
These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 1-Methyl-1H-pyrazole-5-carboxylic acid, its application will become more common.
Reference:
Patent; UCB BIOPHARMA SPRL; BRACE, Gareth Neil; CHAPPELL, Rose Elizabeth; DEBOVES, Herve Jean Claude; FOLEY, Anne Marie; FOULKES, Gregory; JONES, Elizabeth Pearl; LECOMTE, Fabien Claude; QUINCEY, Joanna Rachel; SCHULZE, Monika-Sarah Elisabeth Dorothea; SELBY, Matthew Duncan; SMALLEY, Adam Peter; TAYLOR, Richard David; TOWNSEND, Robert James; ZHU, Zhaoning; (278 pag.)WO2018/229079; (2018); A1;,
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