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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1815959생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1815959

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium hydrideHCID 24758—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물(S)-1-(6-Benzyloxyindazol-1-yl)-propan-2-olHCID 11659201—
용매tetrahydrofuran N,N-dimethylformamideHCID 21974620—
생성물6-Benzyloxy-1-[(S)-2-(tert-butyldimethyl-silanyloxy)-propyl]-1H-indazoleHCID 6957174399%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06881749B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-1670852586064075975c048fc0f6fb16
출처 메모uspto-grants-2005_04