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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Alpha-phenylacetoacetonitrile | HCID 20547 | — |
| 反応物 | 3-Iodopyridine-4-carboxylic acid | HCID 619275 | — |
| 反応物 | 1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-amine | HCID 68819737 | — |
| 触媒 | Cupric acetate | HCID 8895 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-{[1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-yl]amino}isonicotinic acid | HCID 44193429 | 10% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07517878B2 |
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| 出典データセット | uspto-grants-2009_04 |
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| ORD ID | ord-f310d383af404a42a984fc774f7260d8 |
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| 出典メモ | uspto-grants-2009_04 |
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