Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 396724생성일: 2026년 10월 24일
(S)-(-)-N-Benzyl-1-phenylethylamine → methyl 3-{R}-[benzyl-({S}-1-phenyl-ethyl)-amino]-3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)-propionate
https://huagongshe.com/ko/reaction/396724
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (S)-(-)-N-Benzyl-1-phenylethylamine | HCID 1268085 | — |
| 반응물 | Methyl 3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)acrylate | HCID 54398523 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | methyl 3-{R}-[benzyl-({S}-1-phenyl-ethyl)-amino]-3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)-propionate | HCID 21354704 | — |
반응 단계
A solution of (S)-N-benzyl-α-methylbenzylamine (2.6 ml) in anhydrous tetrahydrofuran (50 ml), cooled to −70° C. and under nitrogen, was treated dropwise with a solution of butyllithium in hexanes (5 ml, 2.5M) over about 5 minutes to give a red solution. After stirring at −70° C. for a further 40 minutes the mixture was treated dropwise with a solution of methyl 3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)acrylate [2.0 g, Reference Example 7(d)] in tetrahydrofuran (20 ml) over about 10 minutes. Stirring was continued at low temperature for a further 20 minutes and then the reaction mixture was allowed to warm to room temperature. The mixture was partitioned between ether and water, the layers separated, and the organic layer washed with water then with brine, then dried and then evaporated. The residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and petrol (initially 1:9 and then 15:85, v/v) to give the title compound as a viscous, colourless oil, 1.5 g.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06608084B1 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-f504505246fc43f2b89bbd34262b5278 |
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| 출처 메모 | uspto-grants-2003_08 |
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