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HRID 1521597作成日:2026年10月26日

Sodium bis(trimethylsilyl)amide → 3-Bromo-5-(oxetan-3-YL)pyridine

https://huagongshe.com/reaction/1521597

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物5-Bromopyridine-3-boronic acidHCID 3814811—
反応物Cyclohexanol, 2-amino-, hydrochloride (1:1), (1R,2R)-HCID 12228412—
反応物3-IodooxetaneHCID 13356686—
触媒Nickel(II) iodideHCID 26038—
溶媒IsopropanolHCID 3776—
生成物3-Bromo-5-(oxetan-3-YL)pyridineHCID 72698754—

反応条件

温度80 °C

反応手順

To a vial were added (5-bromopyridin-3-yl)boronic acid (110 mg, 0.544 mmol), nickel iodide (5.10 mg, 0.016 mmol), trans-2-aminocyclohexanol hydrochloride (2.473 mg, 0.016 mmol), sodium bis(trimethylsilyl)amide (100 mg, 0.544 mmol) and 2-propanol (0.5 mL). The reaction was stirred under nitrogen for 10 minutes prior to addition of a solution of 3-iodooxetane (50 mg, 0.27 mmol) in 2-propanol (0.2 mL). The vial was sealed and heated at 80° C. overnight. The reaction was then filtered through celite with the aid of ethanol. The solution was concentrated and purified by flash chromatography on silica gel (10-100% ethyl acetate in hexanes) to provide the title compound: LCMS m/z 215.90 [M+2+H]+; 1H NMR (500 MHz, CD3OD) δ 8.56 (s, 1H), 8.51 (s, 1H), 8.19 (s, 1H), 5.11-5.08 (m, 2H), 4.72-4.70 (m, 2H), 4.34-4.29 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09073929B2
出典データセットuspto-grants-2015_07
ORD IDord-a98b050845b642c2bb492d7a6dcac922
出典メモuspto-grants-2015_07