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HRID 1815959作成日:2026年10月27日

Sodium Iodide → 6-Benzyloxy-1-[(S)-2-(tert-butyldimethyl-silanyloxy)-propyl]-1H-indazole

https://huagongshe.com/reaction/1815959

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Sodium hydrideHCID 24758—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物(S)-1-(6-Benzyloxyindazol-1-yl)-propan-2-olHCID 11659201—
溶媒tetrahydrofuran N,N-dimethylformamideHCID 21974620—
生成物6-Benzyloxy-1-[(S)-2-(tert-butyldimethyl-silanyloxy)-propyl]-1H-indazoleHCID 6957174399%

反応手順

To a mixture of (S)-1-(6-benzyloxyindazol-1-yl)-propan-2-ol (2.03 g, 7.20 mmol) in anhydrous THF/DMF (100 mL/35 mL) under nitrogen was added sodium hydride (60% in mineral oil, 0.40 g, 10.0 mmol). After 30 min tert-butyl-chloro-dimethyl-silane (1.52 g, 10 mmol) and a catalytic amount of NaI were added and the mixture was stirred overnight at ambient temperature. Additional NaH (5 mmol) and tert-butyl-chloro-dimethyl-silane (5 mmol) were added to the reaction mixture, which was stirred for 6 h. The reaction mixture was evaporated to a residue that was mixed with a saturated aqueous solution of sodium bicarbonate and extracted with ethyl acetate (2×200 mL). Purification by chromatography (silica, EtOAc/hexane) gave an oil (2.81 g, 99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06881749B2
出典データセットuspto-grants-2005_04
ORD IDord-1670852586064075975c048fc0f6fb16
出典メモuspto-grants-2005_04