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HRID 571474作成日:2026年10月25日

Cesium carbonate → HCID 71143540、化合物

https://huagongshe.com/reaction/571474

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Methyl 4-bromo-3-fluorobenzoateHCID 21951878—
反応物{3-[4-(7-{[2-(Trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]azetidin-3-yl}acetonitrile dihydrochlorideHCID 67391464—
触媒palladium(II) acetateHCID 167845—
触媒Binap, (A+-)-HCID 634876—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 71143540HCID 71143540104.8%

反応条件

温度120 °C

反応手順

2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (0.11 g, 0.18 mmol) was added to a mixture of {3-[4-(7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]azetidin-3-yl}acetonitrile dihydrochloride (0.86 g, 1.8 mmol), methyl 4-bromo-3-fluorobenzoate (0.50 g, 2.1 mmol, Combi-Blocks: Cat. #CA-4107), and cesium carbonate (1.7 g, 5.4 mmol) in toluene (25.0 mL) under N2, followed by palladium acetate (0.040 g, 0.18 mmol). The reaction mixture was stirred at 120° C. for 5 hours. The reaction mixture was diluted with ethyl acetate, filtered, and concentrated under reduced pressure to afford the desired crude product (1.06 g) which was directly used in next step reaction without further purification. LCMS (M+H)+: m/z=562.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09023840B2
出典データセットuspto-grants-2015_05
ORD IDord-10a55c9bbb22472dbd8536296fa9b04b
出典メモuspto-grants-2015_05