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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8093생성일: 2026년 10월 23일

Triethylamine → [1,1-dimethyl-2-(7-thiophen-3-yl-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/8093

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thiophene-3-boronic acidHCID 581760—
반응물trifluoro-methanesulfonic acid 3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl esterHCID 86595245—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
용매Sodium chloride; waterHCID 57417360—
생성물[1,1-dimethyl-2-(7-thiophen-3-yl-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl esterHCID 6951699569%

반응 단계

To a solution of trifluoro-methanesulfonic acid 3-(2-tert-butoxycarbonylamino-2-methyl-propyl)-1H-indol-7-yl ester (340 mg, 0.779 mmol) in dimethylformamide (5 mL) is added triethylamine (0.14 mL, 1.01 mmol), tetrakis(triphenylphosphine)-palladium (36 mg, 0.0312 mmol) and 3-thiopheneboronic acid (130 mg, 1.01 mmol). The mixture is refluxed for. 22 hours, then cooled and diluted with brine and ethyl acetate. The organic phase is washed 7 times with brine. The 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 198 mg of [1,1-dimethyl-2-(7-thiophen-3-yl-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl ester (69%). FDMS m/e=371 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087635B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-61c1e1a0aa5e442d91a796b5a4f41109
출처 메모uspto-grants-2006_08