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HRID 57104作成日:2026年10月26日

Diisopropylethylamine → Tyclopyrazoflor

https://huagongshe.com/reaction/57104

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Poly(difluoromethylene), alpha-(2-((2-carboxyethyl)thio)ethyl)-omega-fluoro-HCID 171658—
反応物3-chloro-N-ethyl-1-(pyridin-3-yl)-1H-pyrazol-amineHCID 118022192—
溶媒Ethyl AcetateHCID 8857—
生成物TyclopyrazoflorHCID 8670062794%

反応条件

温度27.5 °C

反応手順

A solution of 3-((3,3,3-trifluoropropyl)thio)propanoic acid (2.18 g, 10.8 mmol) and 3-chloro-N-ethyl-1-(pyridine-3-yl)-1H-pyrazol-amine (2.00 g, 8.98 mmol) in ethyl acetate (16 mL) was cooled to 5° C. Diisopropylethylamine (5.15 mL, 29.6 mmol) was added dropwise at 0-5° C. over 30 minutes, followed by the addition of 2,4,6-tripropyl-trioxatriphosphinane-2,4,-trioxide (4.00 g, 12.6 mmol) over 30 minutes at 0-5° C. The reaction was allowed to warm to 25-30° C. and stirred for 2 h. Upon reaction completion, the reaction mixture was cooled to 0-5° C. and quenched with water (12 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (30 mL). The combined organic layers were concentrated to afford the desired product as an oil (3.40 g, 94%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434712B2
出典データセットuspto-grants-2016_09
ORD IDord-1eaec90b3de44e20880eb876a9092e56
出典メモuspto-grants-2016_09