戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 15112作成日:2026年10月26日

2-Bromotoluene → 1-o-tolyl-tetrahydro-1H-pyrrolo[1,2-a]imidazole-2,5-dione

https://huagongshe.com/reaction/15112

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromotolueneHCID 7236—
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
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-o-tolyl-tetrahydro-1H-pyrrolo[1,2-a]imidazole-2,5-dioneHCID 1173636415.4%

反応手順

To a solution of tetrahydro-pyrrolo[1,2-a]imidazole-2,5-dione (1.3 g, 9.28 mmol, prepared as described in J. Med. Chem. 36,4214, 1994) in N-methylpyrrolidone (NMP, 12 cc), CuI (0.5 g, 2.62 mmol), K2CO3 (1.3 g, 9.28 mmol) and 2-bromotoluene (6 g, 35 mmol) were added under stirring. The suspension was heated in a microwave apparatus (250 Watt) for 1 h. 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 Et2O. The solid was filtered, and crystallized the first time with iPrOH and then with AcOEt to yield 0.33 g of the title compound, mp=138-139° 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-a5af9ae55cd3492eb5a25286165b4309
出典メモuspto-grants-2010_06