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HRID 278008作成日:2026年10月27日

4-Chloroquinoline → 5-(Quinolin-4-yl)-3-(1-Methylpiperidin-4-yl)-4-Aza-1H-Indole

https://huagongshe.com/reaction/278008

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChloroquinolineHCID 69140—
反応物Lithium ChlorideHCID 433294—
反応物Potassium FluorideHCID 522689—
反応物HexamethylditinHCID 6327618—
反応物5-Trifluoromethanesulfonyloxy-3-(1-methylpiperidin-4-yl)pyrrolo[3,2-b]pyridineHCID 12041812—
触媒HCID 178418397HCID 178418397—
溶媒1,4-DioxaneHCID 31275—
生成物5-(Quinolin-4-yl)-3-(1-Methylpiperidin-4-yl)-4-Aza-1H-IndoleHCID 986288445.7%

反応条件

温度105 °C

反応手順

O-Trifluoromethanesulfonyl-3-(1-methylpiperidin-4-yl)-5-hydroxy-4-aza-1H-indole (239 mg, 0.658 mmol), tetrakis(triphenylphosphine)palladium(0) (76 mg, 0.065 mmol), dried lithium chloride (167 mg, 3.95 mmol), 4-chloroquinoline (108 mg, 0.658 mmol), hexamethylditin (215 mg, 0.658 mmol), and 15 mL of 1,4-dioxane were placed in a flask and heated to reflux (about 105° C.). The reaction was stirred for about 18 hours before 50 mL of 8M aqueous potassium fluoride solution was added. The solution was extracted with 3:1 chloroform:isopropanol and brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel flash chromatography (0-10% methanol:dichloromethane) to give 103 mg of the title compound. (46%). MS(FD) m/e 343.2 (M+H). EA calculated for C22H22N4: C, 77.16; H, 6.48; N, 16.36. Found: C, 76.98; H, 6.55; N, 16.29.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358972B1
出典データセットuspto-grants-2002_03
ORD IDord-c4f877cb1325475cab04bd5e252084bb
出典メモuspto-grants-2002_03