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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1054765생성일: 2026년 10월 26일

2-Methyl-2-butene → 6-chloro-5-[4-[2-(methylamino)-2-oxoethoxy]phenyl]-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1054765

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-buteneHCID 10553—
반응물Trisodium PhosphateHCID 24243—
반응물Sodium ChloriteHCID 23668197—
반응물2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]-N-methylacetamideHCID 86698756—
용매WaterHCID 962—
용매Acetonitrile tert-butanolHCID 22050040—
생성물6-chloro-5-[4-[2-(methylamino)-2-oxoethoxy]phenyl]-1H-indole-3-carboxylic acidHCID 8669875747.8%

반응 조건

온도0 °C

반응 단계

To a mixture of 2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]-N-methylacetamide (120 mg, 0.35 mmol) in acetonitrile/t-butanol (4 mL/4 mL) was added 2-methyl-2-butene (4 mL). The reaction mixture was cooled to 0° C. followed by the addition of an aqueous solution of sodium chlorite (630 mg, 7.00 mmol) and sodium phosphate (monobasic and monohydrate, 930 mg, 7.00 mmol) in water (5 mL) dropwise via additional funnel. The ice bath was removed and the reaction was stirred at room temperature overnight. The reaction was quenched with sodium sulfite. The reaction mixture was concentrated under reduced pressure and the resulting residue was purified by pre-HPLC to give the title compound (60 mg, 47% yield) as a white solid. MS (ES+) 359.0 (M+H)+. 1H NMR (400 MHz, DMSO-d6) δ 12.12 (s, 1H), 11.94-11.93 (m, 1H), 8.07 (d, 2H), 7.92 (s, 1H), 7.62 (s, 1H), 7.37 (d, 2H), 7.04 (d, 2H), 4.52 (s, 2H), 2.68 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394285B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-bb08ff01798f445d98d14956f78f6b05
출처 메모uspto-grants-2016_07