Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1602913생성일: 2026년 10월 23일
(2S,5S)-2,5-dimethylpiperazine → (2s,5s)-1-(4-Bromo-alpha-(3-(tert-butyldimethylsilyloxy)phenyl)benzyl)-2,5-dimethylpiperazine
https://huagongshe.com/ko/reaction/1602913
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (2S,5S)-2,5-dimethylpiperazine | HCID 61380 | — |
| 반응물 | alpha-(4-Bromophenyl)-3-(tert-butyldimethylsilyloxy)benzyl chloride | HCID 22350043 | — |
| 반응물 | L-Ala-L-Ala diketopiperazine | HCID 131720131 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | (2s,5s)-1-(4-Bromo-alpha-(3-(tert-butyldimethylsilyloxy)phenyl)benzyl)-2,5-dimethylpiperazine | HCID 57043709 | 39% |
반응 단계
The crude benzhydryl chloride (approx. 42 mmol) was combined with 9.55 g (84 mmol) of (+)-(2S,5S)-2,5-dimethylpiperazine, prepared from L-Ala-L-Ala-diketopiperazine (Bachem Chemicals, Philadelphia, Pa.) as described in J. Org. Chem. 50: 4909-13 (1985), and 30 mL of toluene and heated at reflux overnight under nitrogen. The toluene was removed under vacuum, and the residue was redissolved in diethyl ether and washed with 1.0 M sodium hydroxide followed by saturated aqueous sodium chloride. The ether solution was dried over sodium sulfate and the solvent removed to give a dark oil. The product was purified by chromatography on silica gel (Waters Prep 500) with 0.5-0.7% ethanol in dichloromethane with 0.1% triethylamine to give 8.01 g (39%) of (2S,5S)-1-(4-bromo-α-(3-(tert-butyldimethylsilyloxy)phenyl)benzyl)-2,5-dimethylpiperazine as a 1:1 mixture of diastereomers.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05985880 |
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| 출처 데이터셋 | uspto-grants-1999_11 |
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| ORD ID | ord-901068fd391a49e8b2feaf7a44c022d2 |
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| 출처 메모 | uspto-grants-1999_11 |
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