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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2374627생성일: 2026년 10월 26일

Potassium Iodide → (+/-)-8-{3-[1-(2,3-Dihydro-1H-inden-1-yl)-4-piperidinyl]propanoyl}-1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-4-one hydrochloride

https://huagongshe.com/reaction/2374627

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물1-Chloro-2,3-dihydro-1H-indeneHCID 94465—
반응물PotassiumHCID 5462222—
반응물8-[3-(4-piperidinyl)propanoyl]1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-4-oneHCID 9966544—
용매AcetonitrileHCID 6342—
생성물(+/-)-8-{3-[1-(2,3-Dihydro-1H-inden-1-yl)-4-piperidinyl]propanoyl}-1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-4-one hydrochlorideHCID 2188806827.4%

반응 단계

1-Chloroindane (360 mg) was added to a suspension of 8-[3-(4-piperidinyl)propanoyl]1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-4-one (700 mg), potassium carboante (700 mg) and potassium iodide (catalytic amount) in acetonitrile (10 ml) at room temperature, the mixture was stirred for 12 hours, and the reaction mixture was concentrated under reduced pressure. Water (15 ml) and ethyl acetate (20 ml) were added to the residue, and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel chromatography (eluting solvent; ethyl acetate-methanol (9:1)) to give a free base compound of the title compound as colorless crystals (285 mg) having a melting point of 111 to 113° C. The free base compound (270 mg) was treated with a hydrogen chloride-ethanol solution to give the title compound (270 mg) as pale yellow amorphous powders.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07462628B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-c92330da27184475a4c9d29052072674
출처 메모uspto-grants-2008_12