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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338409생성일: 2026년 10월 24일

2-Methyl-2-butene → 6-chloro-5-{4-[2-(morpholin-4-yl)-2-oxoethyl]phenyl}-1H-indole-3-carboxylic acid

https://huagongshe.com/ko/reaction/338409

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-buteneHCID 10553—
반응물Sodium ChloriteHCID 23668197—
반응물Sodium Phosphate, Monobasic, DihydrateHCID 23673460—
반응물6-chloro-5-{4-[2-(morpholin-4-yl)-2-oxoethyl]phenyl}-1H-indole-3-carbaldehydeHCID 86698745—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매tert-ButanolHCID 6386—
생성물6-chloro-5-{4-[2-(morpholin-4-yl)-2-oxoethyl]phenyl}-1H-indole-3-carboxylic acidHCID 8669874628%

반응 조건

온도0 °C

반응 단계

To a solution of 6-chloro-5-{4-[2-(morpholin-4-yl)-2-oxoethyl]phenyl}-1H-indole-3-carbaldehyde (249 mg, 0.650 mmol) in acetonitrile (6 mL) and tert-butanol (6 mL) was added 2-methyl-2-butene (4 mL). The reaction mixture was cooled to 0° C. and treated with a solution of sodium chlorite (880 mg, 13.1 mmol) and sodium phosphate monobasic dihydrate (2030 mg, 13.01 mmol) in water (3 mL) via addition funnel. The icebath was removed and the mixture was allowed to warm to room temperature. The reaction mixture was stirred at room temperature for 18 hours. The reaction was quenched with aqueous sodium sulfite, concentrated in vacuo and extracted with ethyl acetate (4×25 mL). The combined organic phases were washed with brine (20 mL), dried and concentrated in vacuo. The crude product was purified by prep-HPLC (Column: Phenomenex Synergi C18 150*30 mm*4 μm; Mobile phase: from 38% MeCN in water (0.225% FA) to 58% MeCN in water (0.225% FA); Wavelength: 220 nm) to afford the title compound (65 mg, 28% yield) as a white solid. MS (ES+) 399.0 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889730B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-20ceb14a61494f089bae5669b96774bb
출처 메모uspto-grants-2014_11