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HRID 384415作成日:2026年10月25日

p-Toluenesulfonic acid → Methyl 4-iodo-1-tosyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/384415

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物TriethylamineHCID 8471—
反応物methyl 4-iodo-1H-pyrrole-2-carboxylateHCID 11673249—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-iodo-1-tosyl-1H-pyrrole-2-carboxylateHCID 5969442980.2%

反応手順

4-Iodo-1H-pyrrole-2-carboxylic acid methyl ester 57d (25.1 g, 100 mmol) was dissolved in 150 mL of dichloromethane followed by addition of triethylamine (30.6 mL, 220 mmol), 4-dimethylaminopyridine (1.22 g, 10 mmol) and p-toluenesulfonic acid (21 g, 110 mmol). The reaction mixture was reacted at 20° C. overnight. The reaction was monitored by TLC until the disappearance of the starting materials and quenched by addition of 30 mL of hydrochloric acid (1 N). The mixture was extracted with dichloromethane (50 mL×3). The combined organic extracts were washed with saturated aqueous sodium carbonate and saturated brine successively, dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 4-iodo-1-(toluene-4-sulfonyl)-1H-pyrrole-2-carboxylic acid methyl ester 57e (32.5 g, yield 80.2%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367710B2
出典データセットuspto-grants-2013_02
ORD IDord-cada8371c8d248ec8708bec18c1100ae
出典メモuspto-grants-2013_02