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HRID 13102作成日:2026年10月25日

Cesium carbonate → (1R,2S)-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-1-phenylpentan-2-amine

https://huagongshe.com/reaction/13102

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1-(4-fluorophenyl)-5-iodo-1H-indazoleHCID 59251128—
反応物argon (1R,2S)-2-amino-1-phenylpentan-1-ol hydrochlorideHCID 86623008—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒ButyronitrileHCID 8008—
生成物(1R,2S)-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-1-phenylpentan-2-amineHCID 59339774—

反応条件

温度125 °C

反応手順

In a vial under argon (1R,2S)-2-amino-1-phenylpentan-1-ol hydrochloride (91b, 46 mg, 0.21 mmol), 1-(4-fluorophenyl)-5-iodo-1H-indazole (87 mg, 0.26 mmol), copper(I)iodide (8.12 mg, 0.04 mmol) and cesium carbonate (278 mg, 0.85 mmol) were mixed in butyronitrile (0.6 mL). The vial was sealed and heated to 125° C. for 16 h. The mixture was filtered through celite. The celite was washed with ethyl acetate. The collected organic phases were evaporated and the crude product was purified by preparative HPLC. The pure fractions were collected, ethyl acetate and a saturated sodium carbonate were added and the mixture was shaken. The organic layer was separated and the water layer was washed twice with ethyl acetate. The combined organic layers were dried over sodium sulphate and finally evaporated to give the pure product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728030B2
出典データセットuspto-grants-2010_06
ORD IDord-de25f8a7ec5b4322bcb8649f1d574484
出典メモuspto-grants-2010_06