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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1436498생성일: 2026년 10월 27일

(alphaS)-alpha-[Bis(phenylmethyl)amino]benzenepropanal → 2-((2S)-2-Dibenzylamino-1-hydroxy-3-phenylpropyl)-6-ethylpiperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1436498

반응식

참여 물질

역할이름HCID투입량
반응물(alphaS)-alpha-[Bis(phenylmethyl)amino]benzenepropanalHCID 9883943—
반응물tert-Butyl 2-Ethylpiperidine-1-carboxylateHCID 12170201—
반응물CID 53628100HCID 178418400—
용매Diethyl EtherHCID 3283—
생성물2-((2S)-2-Dibenzylamino-1-hydroxy-3-phenylpropyl)-6-ethylpiperidine-1-carboxylic acid tert-butyl esterHCID 69015925—

반응 조건

온도-35 °C

반응 단계

Add N,N,N′,N′-tetrametlhylethylenediamine (1.4 mL, 9.11 mmol), then sec-butyllithium (1.4 M in cyclohexane, 7.2 mL, 10.1 mmol) to 2-ethylpiperidine-1-carboxylic acid tert-butyl ester in diethyl ether (18 mL) at −78° C. under a nitrogen atmosphere. Warm to −35° C. and stir for 1 h. Cool to −78° C. and add (2S)-2-(dibenzylamino)-3-phenylpropanal (3.0 g, 9.11 mmol) in diethyl ether (4 mL) and stir for 30 min. Quench at −78° C. with water, warm to room temperature and extract with diethyl ether. Combine the organic layers, dry (magnesium sulfate) and concentrate. Separate the two major diastereomers of 2-((2S)-2-dibenzylaniino-1-hydroxy-3-phenylpropyl)-6-ethylpiperidine-1-carboxylic acid tert-butyl ester using normal-phase preparative HPLC (Kromasil Si 60, 10 μm, 80×180 mm; 98:2 Hexane:Acetone; 130 mL/min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618978B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-492cf1b5e67a4e8c8cea20c092d44c40
출처 메모uspto-grants-2009_11