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HRID 429267作成日:2026年10月26日

Water → 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(2-imidazolin-2-yl)-4-trifluoromethylsulfinylpyrazole

https://huagongshe.com/reaction/429267

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物EthylenediamineHCID 3301—
反応物FipronilHCID 3352—
反応物Ethyl AcetateHCID 8857—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(2-imidazolin-2-yl)-4-trifluoromethylsulfinylpyrazoleHCID 1835477238.4%

反応手順

5-Amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfinyl-pyrazole (0.81 g, 1.85 mmol) was dissolved in 8 ml of THF, and then ethylenediamine (0.40 ml, 5.98 mmol) was added. The mixture was stirred at room temperature for 1 hour, heated to 50° C. and then stirred for 24 hours. Then, ethylenediamine (0.40 ml, 5.98 mmol) and THF (3 ml) were further added, followed by stirring for 14 hours. After the completion of the reaction, 20 ml of water was added and THF was distilled off and, further, 10 ml of water and 20 ml of an aqueous saturated sodium chloride solution were added. The mixture was extracted twice with 40 ml of ethyl acetate and the ethyl acetate layer was washed twice with 30 ml of an aqueous saturated sodium chloride solution. The resultant was dried over anhydrous magnesium sulfate and then concentrated to obtain a yellow amorphous. The amorphous was subjected to silica gel column chromatography [eluent: mixed solvent of ethyl acetate and hexane (volume ratio=1:2)] to obtain 0.34 g (0.71 mmol) of the title compound as a pale yellow amorphous. Yield 38%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06316477B1
出典データセットuspto-grants-2001_11
ORD IDord-8e84db2929a445b39e3013327c589713
出典メモuspto-grants-2001_11