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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1727136생성일: 2026년 10월 26일

Rolipram → 3-[4-(3-Cyclopentyloxy-4-methoxy-phenyl)-2-oxo-pyrrolidin-1-yl]benzonitrile

https://huagongshe.com/reaction/1727136

반응식

참여 물질

역할이름HCID투입량
반응물RolipramHCID 5092—
반응물3-BromobenzonitrileHCID 23381—
반응물1,2-Diaminocyclohexane, trans-HCID 43806—
반응물Potassium Phosphate, TribasicHCID 62657—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물3-[4-(3-Cyclopentyloxy-4-methoxy-phenyl)-2-oxo-pyrrolidin-1-yl]benzonitrileHCID 1047466996.2%

반응 조건

온도110 °C

반응 단계

A mixture of 4-(3-cyclopentyloxy-4-methoxyphenyl)-pyrrolidin-2-one (1.5 g, 5 mmol), 3-bromobenzonitrile (1.36 g, 7.5 mmol), potassium phosphate (1.9 g, 9.8 mmol), and 1,2-trans-cyclohexanediamine (60 μL) was created in a dry round bottom flask under nitrogen containing DMF (9 mL) and dioxane (9 mL). The mixture was stirred and CuI (100 mg) was added. The resulting reaction mixture was heated to 110° C. with stirring under N2 for 20 h, and then cooled to r.t. The mixture was diluted with EtOAc and then filtered. The filtrate was washed with saturated aqueous solutions of NH4Cl and brine, dried over MgSO4, and concentrated under reduced pressure. Chromatography on silica gel (EtOAc:hexane=1:3 to 1:1) gave 1.81 g of 3-[4-(3-cyclopentyloxy-4-methoxy-phenyl)-2-oxo-pyrrolidin-1-yl]benzonitrile. Yield: 90%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07495016B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-d126f3eed8c14591a419ca2157fcb205
출처 메모uspto-grants-2009_02