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HRID 990743作成日:2026年10月27日

Tetrahydrofuran → Allyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}-3-(5-chloro-1-methyl-3-trifluoromethylpyrazol-4-yl)-3-hydroxyacrylate

https://huagongshe.com/reaction/990743

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物5-Chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonyl chlorideHCID 2794585—
反応物Allyl 2-(3-(2,6-difluorophenyl)pyrazol-1-yl)acetateHCID 22169508—
反応物Potassium butoxideHCID 23699084—
溶媒WaterHCID 962—
生成物Allyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}-3-(5-chloro-1-methyl-3-trifluoromethylpyrazol-4-yl)-3-hydroxyacrylateHCID 86590230—

反応手順

Potassium butoxide (0.5 g) was added to a THF (10 mL) solution of allyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}acetate (0.5 g) and 5-chloro-1-methyl-3-trifluoromethylpyrazole-4-carbonyl chloride (0.44 g) at 0° C. and stirred for 5 minutes. Water (5 ml) was added thereto, and then extracted with diluted hydrochloric acid and ethyl acetate. After the organic layer was dried over anhydrous magnesium sulfate, and then concentrated, and the resulting concentrate was purified through silica gel column chromatography (chloroform) to obtain the intended product, Compound No. I-133 (0.89 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06462049B1
出典データセットuspto-grants-2002_10
ORD IDord-af3d016ba4b84913ad02bef40af1494c
出典メモuspto-grants-2002_10