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HRID 327832作成日:2026年10月25日

Pyrrole-2-Carboxylic Acid → 2-[2-(1H-Pyrrol-2-ylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dione

https://huagongshe.com/reaction/327832

反応式

関与物質

役割名称HCID仕込み量
反応物Pyrrole-2-Carboxylic AcidHCID 12473—
反応物Tin tetrachlorideHCID 24287—
反応物Oxalyl chlorideHCID 65578—
反応物2-(1H-Pyrrol-1-yl)isoindoline-1,3-dioneHCID 853719—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-[2-(1H-Pyrrol-2-ylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dioneHCID 1997317869.2%

反応条件

温度-10 °C

反応手順

To a suspension of pyrrole-2-carboxylic acid (5.55 g) in 500 ml of DCM was added oxalyl chloride (8.7). The reaction mixture was heated under reflux for 1 hour, cooled to -10° C., and tin (IV) chloride (5.85 ml) was added. After stirring the mixture at -10° C. for 30 minutes, 2-(1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)dione (10.6 g) was added in four portions over a period of 30 minutes, followed by stirring at -10° C. for additional 30 minutes. The reaction mixture was then poured into 500 ml of water and extracted with DCM. The combined extracts were washed with 1N sodium hydroxide solution, 1N sulfuric acid, and finally with water. The dried (magnesium sulfate) organic phase was filtered and evaporated in vacuo. The residue was triturated with DCM, affording the product as a powder (10.55 g), mp 204°-206° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05274116
出典データセットuspto-grants-1993_12
ORD IDord-2d0ba08bcd8948fe910437103829fd42
出典メモuspto-grants-1993_12