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HRID 15111作成日:2026年10月27日

Ethyl Acetate → 1-Phenyl-tetrahydro-1H-pyrrolo[1,2-a]imidazole-2,5-dione

https://huagongshe.com/reaction/15111

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物IodobenzeneHCID 11575—
反応物DimiracetamHCID 65955—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物1-Phenyl-tetrahydro-1H-pyrrolo[1,2-a]imidazole-2,5-dioneHCID 1124138611.7%

反応手順

To a solution of tetrahydro-pyrrolo[1,2-a]imidazole-2,5-dione (1 g, 7.14 mmol; prepared as described in J. Med. Chem. 36, 4214-4220, 1994,) in N-methylpyrrolidone (NMP, 12 cc), CuI (0.2 g, 1.05 mmol), K2CO3 (1 g, 7.14 mmol) and Iodobenzene (5 g, 24.5 mmol) were added under stirring. The suspension was heated in a microwave apparatus (250 Watt) for 45 min. Ethyl acetate was added to the suspension and the solid was filtered. The organic phase was washed with water and the aqueous phase was re-extracted with CH2Cl2. The organic phases were gathered and dried over Na2SO4, filtered and concentrated to dryness. The residue was triturated with isopropyl ether. The solid was filtered, triturated with water and filtered to yield 0.18 g of the title compound, mp=185-188° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732473B2
出典データセットuspto-grants-2010_06
ORD IDord-f942b6681ad44b67b36f20f5a2643d6d
出典メモuspto-grants-2010_06