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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15191생성일: 2026년 10월 25일

Sodium hydride → 2-(3-Chloro-4-cyano-2-methylbenzyl)-1-oxo-octahydrocyclopenta[c]-pyrrol-4-yl benzoate

https://huagongshe.com/reaction/15191

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참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-[(3aR,4R,6aS)-4-hydroxy-1-oxo-octahydrocyclopenta[c]pyrrol-2-yl]-2-chloro-3-methylbenzonitrileHCID 11220011—
반응물1-Oxo-octahydrocyclopenta[c]pyrrol-4-yl benzoateHCID 59259560—
반응물4-(Bromomethyl)-2-chloro-3-methylbenzonitrileHCID 68577413—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물2-(3-Chloro-4-cyano-2-methylbenzyl)-1-oxo-octahydrocyclopenta[c]-pyrrol-4-yl benzoateHCID 59259557—
생성물1-(3-Chloro-4-cyano-2-methylbenzyl)-2-oxo-octahydrocyclopenta[b]-pyrrol-4-yl benzoateHCID 59259568—

반응 조건

온도0 °C

반응 단계

To a solution containing mixtures of compound 1I and 1J (170 mg, 0.69 mmol, different batch than previous lot in example 1) in anhydrous THF (4 mL) and anhydrous DMF (4 mL) was added sodium hydride (27.7 mg, 0.69 mmol) at 0° C., and stirred at 0° C. for 45 min. Compound 7C (169 mg, 0.69 mmol) was added at 0° C., the ice-water bath was removed, and the stirring was continued between 0° C. to RT for 2 hr before it was quenched with saturated NH4Cl solution. The mixture was diluted with EtOAc, organic layer was separated, washed with water, dried over MgSO4, and concentrated. Purification by silica gel chromatography (30-100% EtOAc in hexanes) provide the title compound 7D (90 mg) and 7E (151 mg). Compound 7D: (ES) m/z 409 [M+H]+. Compound 7E: (ES) m/z 409 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732480B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-91fdaf33f4db4b739f6eeeb94f2df395
출처 메모uspto-grants-2010_06