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HRID 2109935作成日:2026年10月26日

Potassium Carbonate → 3-{[1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-yl]amino}isonicotinic acid

https://huagongshe.com/reaction/2109935

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Alpha-phenylacetoacetonitrileHCID 20547—
反応物3-Iodopyridine-4-carboxylic acidHCID 619275—
反応物1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-amineHCID 68819737—
触媒Cupric acetateHCID 8895—
溶媒DimethylformamideHCID 6228—
生成物3-{[1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-yl]amino}isonicotinic acidHCID 4419342910%

反応条件

温度150 °C

反応手順

A mixture of 3-iodoisonicotinic acid (180 mg, 0.72 mmol), potassium carbonate (199 mg, 1.44 mmol), 1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-amine (202 mg, 0.72 mmol, synthesized in the same manner as Intermediate F, using commercially available 2-phenylacetoacetonitrile as the nitrile source), and copper (II) acetate (6.5 mg, 0.04 mmol) in DMF (1 mL) was heated (150° C.) in a sealed tube for 16 h. The mixture was cooled to rt, filtered through a silica gel plug using ethyl acetate as eluent, concentrated to dryness, and subjected to HPLC purification using a gradient elution from 30% to 90% acetonitrile in water to afford 29.1 mg (10%) of the desired product. 1H NMR (300 MHz, CD3CN) δ 9.39 (br s, 1H), 7.93 (s, 1H), 7.86-7.90 (m, 2H), 7.05-7.45 (m, 8H), 2.38 (s, 3H), 2.15 (s, 3H); ES-MS m/z 403.1 (MH+), HPLC RT (min) 2.40.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07517878B2
出典データセットuspto-grants-2009_04
ORD IDord-f310d383af404a42a984fc774f7260d8
出典メモuspto-grants-2009_04