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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407607생성일: 2026년 10월 24일

Cesium carbonate → 2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-chlorobenzaldehyde

https://huagongshe.com/ko/reaction/407607

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물EthoxytrimethylsilaneHCID 15772—
반응물2-Chloro-6-fluorobenzaldehydeHCID 67847—
반응물6-(tert-Butyl)-8-fluorophthalazin-1(2H)-oneHCID 59473765—
용매DimethylformamideHCID 6228—
생성물2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-chlorobenzaldehydeHCID 5947382852%

반응 조건

온도60 °C

반응 단계

To a 10 mL round bottom flask were added 6-tert-butyl-8-fluoro-2H-phthalazin-1-one 101h (640 mg, 2.9 mmol), 2-chloro-6-fluorobenzaldehyde (506 mg, 3.2 mmol), and cesium carbonate (488 mg, 1.5 mmol). The flask was evacuated and backfilled with nitrogen three times then ethoxytrimethylsilane (684 mg, 5.8 mmol) and DMF (5 mL) were added to the reaction flask. The resulting mixture was heated to 60° C. After 4 h of stirring, the solution was allowed to cool down to ambient temperature and the reaction was quenched by addition of 2 mL of H2O drop-wise. The desired product started to precipitate from the DMF and water mixture. The solid was collected by filtration after cooling down to 5° C., and washed with DMF/water (2/1, 2 mL, pre-cooled to 6° C.) and H2O (2 mL). The filter cake was dried under vacuum oven at 65° C. for overnight to afford 519 mg (52%) of 101i as a yellow solid. MS: [M+H]+: 359

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754077B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-3593461688bb4cb6901edf0687b528aa
출처 메모uspto-grants-2014_06