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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245953생성일: 2026년 10월 25일

Tributyltin Chloride → 5-(tert-butyldimethylsilyloxy)-1-methyl-3-(tributylstannyl)-1H-indazole

https://huagongshe.com/reaction/245953

반응식

참여 물질

역할이름HCID투입량
반응물Tributyltin ChlorideHCID 15096—
반응물5-((tert-Butyldimethylsilyl)oxy)-3-iodo-1-methyl-1H-indazoleHCID 71279866—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물5-(tert-butyldimethylsilyloxy)-1-methyl-3-(tributylstannyl)-1H-indazoleHCID 71279605—

반응 조건

온도-16 °C

반응 단계

In a round-bottomed flask, 5-(tert-butyl-dimethyl-silanyloxy)-3-iodo-1-methyl-1H-indazole (140 mg, 0.36 mmol) was dissolved in THF (2 ml). The solution was cooled to −16° C. (NaCl/ice bath) and isopropylmagnesium chloride (2.0 M in THF, 0.22 ml, 0.44 mmol) was added dropwise. The reaction mixture was stirred at −16° C. for 20 min then tributylchlorostannane (0.11 ml, 0.41 mmol) was slowly added. The reaction mixture was allowed to warm to room temperature over 1.5 h then quenched with saturated aqueous NH4Cl and extracted with EtOAc (2×). The combined organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated to provide 5-(tert-butyl-dimethyl-silanyloxy)-1-methyl-3-tributylstannanyl-1H-indazole as a light yellow oil which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658646B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-dd8b89f4a9534fd6a6f03935e122a7cd
출처 메모uspto-grants-2014_02