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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225441생성일: 2026년 10월 24일

Sodium Carbonate → 2-(2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-5-pyrazin-2-yl-benzaldehyde

https://huagongshe.com/ko/reaction/225441

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참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물IodopyrazineHCID 642841—
반응물Acetonitrile--water (1/1)HCID 18373917—
반응물2-(2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzaldehydeHCID 76045223—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-5-pyrazin-2-yl-benzaldehydeHCID 8661449939.5%

반응 조건

온도85 °C

반응 단계

To a suspension of 2-(2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzaldehyde (11.5 g, 29.1 mmol) and sodium carbonate (8.8 g, 83.1 mmol) in previously degassed acetonitrile/water (1/1) mixture (140 mL) was added iodopyrazine (5.7 g, 27.7 mmol) under nitrogen. Bis-(triphenylphosphine)-dichloro-palladium-(II) (758 mg, 1.08 mmol) was added at room temperature and the reaction was heated overnight at 85° C. The mixture was cooled to room temperature, diluted with EtOAc and water. The phases were separated and the aqueous phase was re-extracted with EtOAc (×2). The combined organic layers were dried over MgSO4 and concentrated to give a brown oil. Purification on silica gel (hexane/EtOAc 9/1, 8/2 then 7/3) yielded 3.65 g of an off-white solid. 1H-NMR (500 MHz, CDCl3) d 10.35 (s, 1H), 9.06 (t, 1H), 8.70 (dd, 1H), 8.57 (d, 1H) 8.32 (dd, 1H), 4.24 (m, 2H), 3.43 (dt, 2H), 3.05 (m, 2H), 1.32 (d, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557100B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-957aa693d47148a5b2ceebf72c6906e5
출처 메모uspto-grants-2009_07