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Water → 2-(1-(2-Fluoro-4-nitrophenyl)-3-pyrazolyl)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1,2-Difluoro-4-nitrobenzene | HCID 123053 | — |
| 反応物 | 2-(1H-Pyrazol-3-Yl)Pyridine | HCID 2797657 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(1-(2-Fluoro-4-nitrophenyl)-3-pyrazolyl)pyridine | HCID 86719370 | 93.4% |
反応手順
Compound 17a (1 g, 6.9 mmol) obtained from the aforesaid process and 3,4-difluoro-nitrobenzene (0.74 mL) were dissolved in N,N-dimethylformamide (20 mL), and then anhydrous potassium carbonate (1.9 g) was added thereto. The mixture was reacted at 100° C. for 4 hours. After completion of the reaction, the reactant mixture was cooled to room temperature. Water was added to the mixture, resulting in a substantial amount of precipitate. Then, the precipitate was suction-filtered, and the filter cake was recrystallized with acetone to get the product 18a as a white powder (1.7 g), with a yield of 93.4%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08946436B2 |
| 出典データセット | uspto-grants-2015_02 |
| ORD ID | ord-4e1a3b5185124e079c66a717fc1b1ff5 |
| 出典メモ | uspto-grants-2015_02 |