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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1683990생성일: 2026년 10월 27일

Hydrogen Peroxide → 4-(1-(4-Bromobenzyl)-5-methoxy-2-methyl-1H-indol-3-yl)-3-methylbutanoic acid

https://huagongshe.com/reaction/1683990

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Lithium HydroxideHCID 3939—
반응물(4R)-N-[4-(1-(4-Bromobenzyl)-5-methoxy-2-methyl-1H-indol-3-yl)-3-methylbutanoyl]-4-isopropyl-2-oxazolidinoneHCID 54133645—
용매TetrahydrofuranHCID 8028—
생성물4-(1-(4-Bromobenzyl)-5-methoxy-2-methyl-1H-indol-3-yl)-3-methylbutanoic acidHCID 9867333—

반응 조건

온도0 °C

반응 단계

To the oxazolidinone from Step 7, isomer A (295 mg, 0.54 mmol) in THF (10 mL) at -10° C. was added 30% H2O2 (0.5 mL) followed by 1M aqueous LiOH (3 mL). The mixture was stirred at 0° C. for 45 min, and was then cooled to -10° C. to be quenched by careful addition of 1M aqueous Na2S2O5 (10 mL). The mixture was acidified (6M HCl, 1 mL) and the product was extracted with EtOAc. The organic layer was washed with H2O and brine, and was then dried (MgSO4), and filtered. After removal of the solvent, the crude product was purified by flash chromatography (1:5 EtOAc/hexane followed by 1:2 EtOAc/hexane). The resulting off-white solid was stirred vigorously with 1:10 EtOAc/hexane for 2 h to give, after filtration, 188 mg of the title compound. [α]D =+4.6° (c=1, acetone)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05639780
출처 데이터셋uspto-grants-1997_06
ORD IDord-4582306753c74139b39e5a5ea654d00c
출처 메모uspto-grants-1997_06