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HRID 1914527作成日:2026年10月27日

Cesium carbonate → 2-Pyrrolidin-1-yl-6-(4-trifluoromethyl-phenyl)-isonicotinonitrile

https://huagongshe.com/reaction/1914527

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4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
反応物2-Chloro-6-(pyrrolidin-1-yl)pyridine-4-carbonitrileHCID 83074580—
触媒palladium(II) acetateHCID 167845—
触媒2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
溶媒1,4-DioxaneHCID 31275—
生成物2-Pyrrolidin-1-yl-6-(4-trifluoromethyl-phenyl)-isonicotinonitrileHCID 6683235592%

反応条件

温度100 °C

反応手順

2-Chloro-6-pyrrolidin-1-yl-isonicotinonitrile (0.18 g, 0.87 mmol), 4-trifluoromethylphenylboronic acid (0.18 g, 0.95 mmol), palladium acetate (3.9 mg, 0.02 mmol), cesium carbonate (0.56 g, 1.73 mmol), and XPhos (17 mg, 0.04 mmol) were combined, placed under a nitrogen atmosphere and dioxane (1.0 mL) was added. The reaction vessel was sealed and heated to 100° C. for 2 hours. The reaction mixture was cooled to rt, filtered through celite, concentrated under reduced pressure and purified by flash column chromatography (0%-80% EtOAc in hexane) to provide the desired product (253 mg, 92%). 1H NMR (400 MHz, CDCl3) δ 8.11 (d, J=8.1 Hz, 2H), 7.70 (d, J=8.2 Hz, 2H), 7.15 (d, J=0.8 Hz, 1H), 6.54 (d, J=0.9 Hz, 1H), 3.55 (bs, 4H), 2.13-1.99 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08614201B2
出典データセットuspto-grants-2013_12
ORD IDord-6a7a22c1c5774919996decbdd2dafcfb
出典メモuspto-grants-2013_12