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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1106929생성일: 2026년 10월 25일

Trifluoroacetic acid → (1R,3S)-benzyl 1-(1-adamantyl)methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]-indole-3-carboxylate

https://huagongshe.com/reaction/1106929

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물2-(Adamantan-1-yl)acetaldehydeHCID 5086084—
반응물L-Tryptophan benzyl esterHCID 7016092—
반응물Dichloromethane ethylacetateHCID 21226138—
용매DichloromethaneHCID 6344—
생성물(1R,3S)-benzyl 1-(1-adamantyl)methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]-indole-3-carboxylateHCID 10551689—

반응 단계

Trifluoroacetic acid (270 μl, 3.5 mmol) was added to a solution of L-tryptophan benzyl ester (10.23 g, 34.8 mmol) and 1-adamantylacetaldehyde (6.2 g, 34.8 mmol) in dry DCM (300 ml) wth 3A molecular sieves (46.5 g) at -10° C. The reaction mixture was allowed to warm to room temperature and stirred for 7 hours. The mixture was cooled to 0° C. trifluoroacetic acid (5.6 ml, 72.7 mmol) added, and stirring continued at room temperature for 16 hours. The reaction mixture was filtered, washed successively with saturated NaHCO3 solution (200 ml), brine (2×200 ml) and dried (MgSO4). Filtration and evaporation of the solvent gave the crude product. The compound was obtained by isolation of the more polar component by flash chromatography on silica gel with ethyl acetate-DCM (1:40) as eluant. (6.2 g, 39%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06057311
출처 데이터셋uspto-grants-2000_05
ORD IDord-d3600634d0a145f38dd566702bcc0cb8
출처 메모uspto-grants-2000_05