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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1667127생성일: 2026년 10월 27일

3,3-Diphenylpyrrolidine → 1-[2-(3,3-Diphenylpyrrolidin-1-yl)-2-oxoethyl]-3,3-bis(4-fluorophenyl)pyrrolidin-2-one

https://huagongshe.com/reaction/1667127

반응식

참여 물질

역할이름HCID투입량
반응물3,3-DiphenylpyrrolidineHCID 418242—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(3,3-Bis(4-fluorophenyl)-2-oxopyrrolidin-1-yl)acetic acidHCID 67357191—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물1-[2-(3,3-Diphenylpyrrolidin-1-yl)-2-oxoethyl]-3,3-bis(4-fluorophenyl)pyrrolidin-2-oneHCID 67359459—

반응 단계

To a solution of 3,3-diphenylpyrrolidine (Example 17A, 0.22 g, 1.00 mmol) in dichloromethane (25 mL) under nitrogen was added 2-(3,3-bis(4-fluorophenyl)-2-oxopyrrolidin-1-yl)acetic acid (Example 58D, 0.33 g, 1.00 mmol) followed by N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (0.39 g, 2.00 mmol) and N,N-dimethylpyridin-4-amine (0.012 g, 0.10 mmol). The reaction mixture was stirred overnight at room temperature. The reaction was concentrated and the residue was partitioned in ethyl acetate/water (8:2). The organic layer was washed with water followed by brine, dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography eluting with 3% methanol/dichloromethane gave the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 7.14-7.36 (m, 14H), 6.95-7.01 (m, 4H), 4.22 (s, 1H), 4.17 (s, 1H), 4.10 (s, 1H), 4.08 (s, 1H), 3.51-3.60 (m, 3H), 3.42 (t, J=6.7 Hz, 1H), 2.72-2.80 (m, 2H), 2.62 (t, J=6.6 Hz, 1H), 2.53 (t, J=6.8 Hz, 1H); MS (DCI+) m/z 537 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044069B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-a6444c8f10e14e61ba3143d43e9c6dbf
출처 메모uspto-grants-2011_10