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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2109935생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2109935

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Alpha-phenylacetoacetonitrileHCID 20547—
반응물3-Iodopyridine-4-carboxylic acidHCID 619275—
반응물1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-amineHCID 68819737—
촉매Cupric acetateHCID 8895—
용매DimethylformamideHCID 6228—
생성물3-{[1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-yl]amino}isonicotinic acidHCID 4419342910%

반응 조건

온도150 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07517878B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-f310d383af404a42a984fc774f7260d8
출처 메모uspto-grants-2009_04