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HRID 407607作成日:2026年10月25日

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

https://huagongshe.com/reaction/407607

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物EthoxytrimethylsilaneHCID 15772—
反応物2-Chloro-6-fluorobenzaldehydeHCID 67847—
反応物6-(tert-Butyl)-8-fluorophthalazin-1(2H)-oneHCID 59473765—
溶媒DimethylformamideHCID 6228—
生成物2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-chlorobenzaldehydeHCID 5947382852%

反応条件

温度60 °C

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754077B2
出典データセットuspto-grants-2014_06
ORD IDord-3593461688bb4cb6901edf0687b528aa
出典メモuspto-grants-2014_06