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HRID 73247作成日:2026年10月24日

1-Hydroxybenzotriazole → N-[(1-methylpyrrolidin-2-yl)ethyl]-5-formyl-2,4-dimethyl-1H-pyrrole-3-formamide

https://huagongshe.com/ja/reaction/73247

反応式

関与物質

役割名称HCID仕込み量
反応物1-HydroxybenzotriazoleHCID 75771—
反応物2-(2-Aminoethyl)-1-methylpyrrolidineHCID 98388—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic AcidHCID 11073792—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
生成物N-[(1-methylpyrrolidin-2-yl)ethyl]-5-formyl-2,4-dimethyl-1H-pyrrole-3-formamideHCID 8665913750.2%

反応条件

温度0 °C

反応手順

1-Ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride (268.1 g, 1.4 mol), triethylamine (280.0 mL), 5-formyl-2,4-dimethyl-1H-pyrrole-3-formic acid (167.0 g, 1.0 mol) and 1-hydroxybenzotriazole (189.2 g, 1.4 mol) were sequentially added to DMF (500 mL) with stirring at about 0° C., and stirred for 1.5 hrs, then (1-methylpyrrolidin-2-yl)ethylamine (1.2 mol) was added. The reaction was stirred at room temperature until completion was indicated by thin layer chromatography (TLC). 120 mL of water and 100 mL of saturated salt water were added, and the mixture was extracted with 10% methanol/dichloromethane (300 mL×3), the combined organic phase was washed with saturated salt water (300 mL×3), dried over anhydrous Na2SO4, and the solvent was distilled off under reduced pressure. The residue was then chromatographed on silica gel (eluted with methanol/ethyl acetate=1/1) to give 139.1 g (502 mmol) of N-[(1-methylpyrrolidin-2-yl)ethyl]-5-formyl-2,4-dimethyl-1H-pyrrole-3-formamide as an off-white solid. Yield 50.2%, m.p. 143-149° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829039B2
出典データセットuspto-grants-2014_09
ORD IDord-c45367a4b6c043bb99cd934a8bbe4033
出典メモuspto-grants-2014_09