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HRID 1011616作成日:2026年10月27日

4-(Trifluoromethyl)benzenesulfonamide → N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methylene)-4-(trifluoromethyl)benzenesulfonamide

https://huagongshe.com/reaction/1011616

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Trifluoromethyl)benzenesulfonamideHCID 70018—
反応物3-Iodo-1-(methoxymethyl)-1H-pyrazole-4-carbaldehydeHCID 57659764—
触媒Titanium tetraethoxideHCID 76524—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methylene)-4-(trifluoromethyl)benzenesulfonamideHCID 67313312—

反応手順

3-Iodo-1-(methoxymethyl)-1H-pyrazole-4-carbaldehyde (39) (2.0 g, 7.52 mmol) and 4-(trifluoromethyl)benzenesulfonamide (40) (1.69 g, 7.52 mmol) were dissolved in THF (20 mL) under nitrogen. Titanium(IV) ethoxide (7.8 mL, 37.6 mmol) was added via syringe and the reaction stirred for 16 hr at rt. The reaction was poured into brine (50 mL) and filtered through a pad of Celite. The filtrate was extracted with EtOAc (3×50 mL) and the combined organics were washed with brine (100 mL), dried over Na2SO4, and concentrated in vacuo to give N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methylene)-4-(trifluoromethyl)benzenesulfonamide (41) as a clear oil that was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07977368B2
出典データセットuspto-grants-2011_07
ORD IDord-18b12a13eaee4612ab3c910786c31e50
出典メモuspto-grants-2011_07