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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8092생성일: 2026년 10월 23일

Sodium Carbonate → {1,1-dimethyl-2-[7-(4-trifluoromethyl-phenyl)-1H-indol-3-yl]-ethyl}-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/8092

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
반응물trifluoro-methanesulfonic acid 3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl esterHCID 86595245—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물{1,1-dimethyl-2-[7-(4-trifluoromethyl-phenyl)-1H-indol-3-yl]-ethyl}-carbamic acid tert-butyl esterHCID 6951791193.3%

반응 단계

To a solution of trifluoro-methanesulfonic acid 3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl ester (305 mg, 0.699 mmol) in tetrahydrofuran (4.5 mL) is added sodium carbonate (1 mL, 2M, 2 mmol), tetrakis(triphenylphosphine)-palladium (32 mg, 0.0280 mmol) and 4-trifluoromethylbenzeneboronic acid (0.1 99 g, 1.05 mmol). The mixture is refluxed for 22 hours, then cooled, diluted with brine and extracted three times with ethyl acetate. The combined organics are dried over anhydrous sodium sulfate, filtered and then evaporated in vacuo. The residue is purified using silica gel chromatography (hexane/20% ethyl acetate, hexane gradient elution) to give 282 mg of {1,1-dimethyl-2-[7-(4-trifluoromethyl-phenyl)-1 H-indol-3-yl]-ethyl}-carbamic acid tert-butyl ester (93%). FDMS m/e=433 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087635B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-1bf2a222fc824b4c96663fff97db984b
출처 메모uspto-grants-2006_08