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HRID 85036作成日:2026年10月26日

1H-Pyrrolo(2,3-b)pyridine → 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/85036

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Pyrrolo(2,3-b)pyridineHCID 9222—
反応物Sodium hydrideHCID 24758—
反応物2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
溶媒DimethylformamideHCID 6228—
生成物1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridineHCID 58431351100.6%

反応条件

温度0 °C

反応手順

To a stirred solution of 7-azaindole (1.18 g, 10.0 mmol) in anhydrous dimethylformamide (10 mL) cooled to 0° C. was added NaH [60% dispersion in mineral oil](0.480 g, 12.0 mmol) in portions over 15 min. The resulting mixture was allowed to stir for 1 hr at 0° C., after which (2-(chloromethoxy)ethyl)trimethylsilane [SEM-Cl] (2.12 mL, 12.0 mmol) was added over 15 min. The resulting mixture was stirred for 1 hr, after which it was quenched with H2O (50 mL), and partioned between EtOAc and H2O. The organic layer was separated, washed with brine, dried over MgSO4, filtered, and evaporated in vacuo to yield a yellow oil (2.50 g, 100%). HPLC retention time: 2.66 minutes; MS ESI (m/z): 249.4 (M+1)+, calc. 248.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846909B2
出典データセットuspto-grants-2014_09
ORD IDord-91f4e083c1914a8784c70848a1633c2b
出典メモuspto-grants-2014_09