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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77360생성일: 2026년 10월 23일

Toluene → 6-methyl-3-(4-trifluoromethyl-phenyl)-2H-pyrrolo[1,2-a]pyrazin-1-one

https://huagongshe.com/ko/reaction/77360

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물2-(Dimethylamino)ethanolHCID 7902—
반응물6-bromo-3-(4-trifluoromethyl-phenyl)-2H-pyrrolo[1,2-a]pyrazin-1-oneHCID 72715043—
반응물HCID 178477796HCID 178477796—
용매TetrahydrofuranHCID 8028—
생성물6-methyl-3-(4-trifluoromethyl-phenyl)-2H-pyrrolo[1,2-a]pyrazin-1-oneHCID 7255129534.2%

반응 조건

온도50 °C

반응 단계

A mixture of 6-bromo-3-(4-trifluoromethyl-phenyl)-2H-pyrrolo[1,2-a]pyrazin-1-one (Example 128) (0.1 g, 0.28 mmol), 1,1′-bis(diphenylphosphino)ferrocenedichloro palladium(II) dichloromethane complex (61.5 mg, 84.0 μmol) and N,N-dimethylethanolamine (14.1 μL, 140 μmol) in tetrahydrofuran (1.5 mL) under argon was treated with 1.2M dimethylzinc in toluene (280 μL, 0.33 mmol). The reaction mixture was stirred in a sealed vial at 50° C. overnight. At this time, the reaction was treated with additional dimethylzinc (0.14 mL). The reaction mixture was stirred at 50° C. over the weekend. At this time, the reaction mixture was cooled to room temperature, quenched with a saturated aqueous ammonium chloride solution and then extracted with ethyl acetate. Methanol (0.5 mL) was added, the mixture was filtered and the layers were separated. The organic layers were absorbed onto silica gel. Flash chromatography (12 g silica column, 0-40% ethyl acetate/hexanes) followed by trituration with methylene chloride afforded 6-methyl-3-(4-trifluoromethyl-phenyl)-2H-pyrrolo[1,2-a]pyrazin-1-one (14 mg, 17%) as white solid. 1H NMR (methanol-d4) δ ppm 7.76-7.86 (m, 4H), 7.69 (s, 1H), 7.28 (s, 1H), 6.95, (s, 1H), 2.28 (s, 3H). LC-MS calcd. for C15H12F3N2O [(M+H)+] 293, obsd. 293.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841299B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-fb199b2425d74e3399272de095929b83
출처 메모uspto-grants-2014_09