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HRID 6958作成日:2026年10月23日

Triethylamine → Methyl 5-sulfamoylthiophene-2-carboxylate

https://huagongshe.com/ja/reaction/6958

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl AcetateHCID 8857—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物5-Bromo-2-thiophenesulfonamideHCID 1241304—
反応物HCID 178418416HCID 178418416—
触媒palladium(II) acetateHCID 167845—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物Methyl 5-sulfamoylthiophene-2-carboxylateHCID 13425727—

反応条件

温度100 °C

反応手順

A mixture of 5-bromothiophene-2-sulfonamide (0.50 g, 2.1 mmol), triethyl amine (1 mL), methanol (1 mL), palladium acetate (0.046 g, 2.1 mmol) and 1,3-bis(diphenylphosphino) propane (0.085 g, 2.1 mmol) (addition in that order) in dimethylformamide (5 mL, anhydrous) is saturated with carbon monoxide gas, at room temperature. This reaction mixture is heated to 100° C. and stirred overnight, under a carbon monoxide atmosphere. 10 mL of brine and 10 mL of ethyl acetate are added to the reaction mixture. The organic phase is separated and the aqueous layer is extracted with 10 mL ethyl acetate. The combined organic layers are dried over sodium sulfate, concentrated in vacuo, and then chromatographed on silica (0–1% methyl alcohol in methylene chloride) to give the title compound, as a yellow solid (0.15 g, 34% 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-7b3ef08a6ec846058fe20b3dbccc2c1d
出典メモuspto-grants-2006_08