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HRID 1822644作成日:2026年10月26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/1822644

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US07037880B2
出典データセットuspto-grants-2006_05
ORD IDord-1b13ba0bcd2e41769c1748fcfab9e61a
出典メモuspto-grants-2006_05