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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53222생성일: 2026년 10월 25일

Water → 2-[4-[4-(2-Methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-butyl]-7-azaindole

https://huagongshe.com/reaction/53222

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylsilaneHCID 12052—
반응물Sodium BicarbonateHCID 516892—
반응물2-[4-[4-(2-Methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-1-hydroxy-butyl]-7-azaindoleHCID 19082014—
용매Trifluoroacetic acidHCID 6422—
생성물2-[4-[4-(2-Methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-butyl]-7-azaindoleHCID 1908201974%

반응 조건

온도20 °C

반응 단계

Triethylsilane (5 ml) was added to a stirred solution of 2-[4-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-1-hydroxy-butyl]-7-azaindole (520 mg, 1.33 mmol) in 20 ml of trifluoroacetic acid at 20° C. under nitrogen. The mixture was stirred at 20° C. for 10 min and then stirred at 70°-75° C. for 16 h. To the mixture was added water, and basified with an aqueous sodium bicarbonate solution (to pH=8) followed by extraction with methylene chloride (3x). The combined organic layer was dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica column chromatography (7.5 cm column, ethyl acetate/hexane, 1/5-8/1) . The mixture was recrystallized to afford 349 mg (74%) of 2-[4-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-butyl]-7-azaindole, as a white solid, m.p. 147°-150° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618821
출처 데이터셋uspto-grants-1997_04
ORD IDord-bfb4f366bccc4afb8e8ffb785b490cc5
출처 메모uspto-grants-1997_04