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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339640생성일: 2026년 10월 24일

Potassium Carbonate → 2-(1-(bis(4-fluorophenyl)methyl)piperidin-4-ylidene)-N-(cyclopropylmethyl)acetamide

https://huagongshe.com/ko/reaction/339640

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1,1'-(Chloromethylene)bis(4-fluorobenzene)HCID 2723773—
반응물N-(cyclopropylmethyl)-2-(piperidin-4-ylidene)acetamide hydrochlorideHCID 66680987—
용매AcetonitrileHCID 6342—
생성물2-(1-(bis(4-fluorophenyl)methyl)piperidin-4-ylidene)-N-(cyclopropylmethyl)acetamideHCID 5806533578%

반응 단계

A mixture of N-(cyclopropylmethyl)-2-(piperidin-4-ylidene)acetamide hydrochloride (80.0 mg, 0.347 mmol) prepared in EXAMPLE 22e, 4,4′-difluorobenzhydryl chloride (0.105 ml, 0.555 mmol), K2CO3 (105 mg, 0.763 mmol) and KI (5.8 mg, 0.035 mmol) in acetonitrile (5 ml) was stirred under reflux for 12 hours. The reaction was quenched with H2O (20 ml), extracted with chloroform (30 ml×2), dried over MgSO4 and concentrated in vacuo. The residue was purified by column chromatography (ethyl acetate/hexane:30/70 to 50/50) to give 2-(1-(bis(4-fluorophenyl)methyl)piperidin-4-ylidene)-N-(cyclopropylmethyl)acetamide (107 mg, 78%) as a white solid: LCMS: 397 {M+1}+. 1H NMR (DMSO-d6)□ δ: 0.11 (m, 2H), 0.38 (m, 2H), 0.87 (m, 1H), 2.22 (m, 2H), 2.32 (m, 2H), 2.36 (m, 2H), 2.93 (m, 4H), 4.47 (s, 1H), 5.61 (s, 1H), 7.13 (m, 4H), 7.43 (m, 4H), 7.87 (t, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895551B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-4e4cc702a59d468fb8dd047f8bd17543
출처 메모uspto-grants-2014_11