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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

반응식

참여 물질

역할이름HCID투입량
반응물(S)-(-)-N-Benzyl-1-phenylethylamineHCID 1268085—
반응물Methyl 3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)acrylateHCID 54398523—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물methyl 3-{R}-[benzyl-({S}-1-phenyl-ethyl)-amino]-3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)-propionateHCID 21354704—

반응 조건

온도-70 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608084B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-f504505246fc43f2b89bbd34262b5278
출처 메모uspto-grants-2003_08