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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8105생성일: 2026년 10월 24일

Methyl Acrylate → 3-[3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl]-acrylic acid methyl ester

https://huagongshe.com/ko/reaction/8105

반응식

참여 물질

역할이름HCID투입량
반응물Methyl AcrylateHCID 7294—
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물trifluoro-methanesulfonic acid 3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl esterHCID 86595245—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물3-[3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl]-acrylic acid methyl esterHCID 6951784682%

반응 조건

온도90 °C

반응 단계

Trifluoro-methanesulfonic acid 3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl ester (200 mg, 0.46 mmol), methyl acrylate (80 mg, 0.92 mmol) and triethylamine (0.40 mL, 3.0 mmol) is stirred in dimethylformamide (2.0 mL) at room temperature for 30 minutes. Dichlorobis(triphenylphosphine)palladium (31 mg, 0.045 mmol) is added, the reaction mixture is heated to 90° C. and allowed to stir overnight. The reaction is cooled to room temperature, poured into a separatory funnel containing ethyl acetate and brine (50 mL each) and the aqeous layer is extracted with ethyl acetate (50 mL). The combined organic layers are washed with brine, dried (Na2SO4) and evaporated. The residue is purified using silica gel chromatography (20% ethyl acetate/hexane) to give 140 mg of 3-[3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl]-acrylic acid methyl ester (82%). FDMS mie =372.2 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087635B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d71cbd8395f942d6899bd3f39091693f
출처 메모uspto-grants-2006_08