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HRID 1092253作成日:2026年10月25日

2,3,4,5-Tetrafluoronitrobenzene → 5-cyclopropyl-N-(2,3,4-trifluoro-6-nitrophenyl)-1H-pyrazol-3-amine

https://huagongshe.com/reaction/1092253

反応式

関与物質

役割名称HCID仕込み量
反応物2,3,4,5-TetrafluoronitrobenzeneHCID 79691—
反応物DiisopropylethylamineHCID 81531—
反応物3-cyclopropyl-1H-pyrazol-5-amineHCID 2758014—
溶媒TetrahydrofuranHCID 8028—
生成物5-cyclopropyl-N-(2,3,4-trifluoro-6-nitrophenyl)-1H-pyrazol-3-amineHCID 8607980216%

反応条件

温度25 °C

反応手順

To 1,2,3,4-tetrafluoro-5-nitrobenzene (3.0 g, 15.4 mmol) and DIEA (3.7 ml, 21.0 mmol) in dry THF (20 ml) was added 5-cyclopropyl-1H-pyrazol-3-amine (1.7 g, 14.0 mmol) in THF (5 ml) drop wise at 0° C. After addition, the reaction mixture was stirred at 25° C. for 16 hours. The solvent was removed under reduced pressure and the resulted residue was purified by column chromatography (hexane-EtOAc=4:1). This was recrystallized from Et2O (20 ml) and hexanes (˜150 ml) to give the title compound as red crystals (0.650 g, 16%). 1H NMR (400 MHz) 11.84 (s, 1H), 8.67 (s, 1H), 8.06 (m, 1H), 5.57 (s, 1H), 1.82 (m, 1H), 0.89 (m, 2H), 0.65 (m, 2H). MS: Calcd.: 298; Found: [M+H]+ 299.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129403B2
出典データセットuspto-grants-2012_03
ORD IDord-1eb80a444fff4110ae29f0834f9a65b6
出典メモuspto-grants-2012_03