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HRID 1081237作成日:2026年10月23日

Hydrochloric Acid → N-(1,1-Dimethylethyl)-1-methyl-2-(methylthio)-1H-pyrrole-3-sulfonamide

https://huagongshe.com/ja/reaction/1081237

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Dimethyl DisulfideHCID 12232—
反応物N-(1,1-Dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamideHCID 19693811—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物N-(1,1-Dimethylethyl)-1-methyl-2-(methylthio)-1H-pyrrole-3-sulfonamideHCID 1969381458.8%

反応条件

温度-78 °C

反応手順

To a solution of 6.48 g (30 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 150 mL THF under nitrogen atmosphere cooled to -78° C. was added dropwise at such a rate as to keep the temperature below -65° C. 25.52 mL (61.5 mmol) 2.41M n-butyllithium in hexanes. The reaction was stirred at -78° C. for ca. 30 minutes. To the reaction mixture was added 2.97 mL (33 mmol) of dimethyldisulfide in one portion and the resulting reaction mixture was allowed to warm to room temperature and stir for ca. 1.5 hours. The reaction mixture was cooled to 0° C. and acidified with 1N HCl. The THF phase was separated washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue was chromatographed on silica (20% ethyl acetate/80% hexanes) affording 4.63 g of the title compound as an off white solid, m.p. 116°-119° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05585328
出典データセットuspto-grants-1996_12
ORD IDord-31047b9f15c44866bc8f9dfa791fd7b4
出典メモuspto-grants-1996_12