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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (alphaS)-alpha-[Bis(phenylmethyl)amino]benzenepropanal | HCID 9883943 | — |
| 반응물 | tert-Butyl 2-Ethylpiperidine-1-carboxylate | HCID 12170201 | — |
| 반응물 | CID 53628100 | HCID 178418400 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2-((2S)-2-Dibenzylamino-1-hydroxy-3-phenylpropyl)-6-ethylpiperidine-1-carboxylic acid tert-butyl ester | HCID 69015925 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07618978B2 |
|---|
| 출처 데이터셋 | uspto-grants-2009_11 |
|---|
| ORD ID | ord-492cf1b5e67a4e8c8cea20c092d44c40 |
|---|
| 출처 메모 | uspto-grants-2009_11 |
|---|