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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | 2-(Adamantan-1-yl)acetaldehyde | HCID 5086084 | — |
| 반응물 | L-Tryptophan benzyl ester | HCID 7016092 | — |
| 반응물 | Dichloromethane ethylacetate | HCID 21226138 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (1R,3S)-benzyl 1-(1-adamantyl)methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]-indole-3-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06057311 |
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| 출처 데이터셋 | uspto-grants-2000_05 |
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| ORD ID | ord-d3600634d0a145f38dd566702bcc0cb8 |
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| 출처 메모 | uspto-grants-2000_05 |
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