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HRID 6957作成日:2026年10月24日

Methanol → 5-Cyanothiophene-2-sulfonamide

https://huagongshe.com/ja/reaction/6957

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物WaterHCID 962—
反応物DimethylformamideHCID 6228—
反応物Ethyl AcetateHCID 8857—
反応物5-Bromo-2-thiophenesulfonamideHCID 1241304—
触媒Zinc cyanide (Zn(CN)2)HCID 11186—
触媒HCID 178418397HCID 178418397—
溶媒DichloromethaneHCID 6344—
生成物5-Cyanothiophene-2-sulfonamideHCID 22019526—

反応手順

A mixture of 5-bromothiophene-2-sulfonamide (0.50 g, 2.1 mmol), zinc cyanide (0.25 g, 2.1 mmol), tetrakis(triphenylphosphine)palladium(0) (0.072 g, 0.06 mmol) in dimethylformamide (5 mL, anhydrous) is placed under microwave radiation (under nitrogen atmosphere, 160° C.) for 15 min. Thin layer chromatography (5% methyl alcohol in methylene chloride) demonstrates the reaction is incomplete. Additional tetrakis-(triphenylphosphine)palladium(0) (0.24 g, 0.2 mmol) and dimethylformamide (10 mL) are added to the reaction mixture and placed under microwave radiation (under nitrogen atmosphere at 160° C.) for 37 min. 10 mL of water and 20 mL of ethyl acetate are added to the reaction mixture. The organic phase is separated and the aqueous layer is extracted with 20 mL ethyl acetate. The combined organic layers are dried over sodium sulfate, concentrated in vacuo, and then chromatographed on silica (0–5% methyl alcohol in methylene chloride) to give the title compound, as a white solid (0.22 g, 57% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084170B2
出典データセットuspto-grants-2006_08
ORD IDord-c726936bb48143acb2070697d2b01b54
出典メモuspto-grants-2006_08