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HRID 1602913作成日:2026年10月23日
(2S,5S)-2,5-dimethylpiperazine → (2s,5s)-1-(4-Bromo-alpha-(3-(tert-butyldimethylsilyloxy)phenyl)benzyl)-2,5-dimethylpiperazine
https://huagongshe.com/ja/reaction/1602913
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (2S,5S)-2,5-dimethylpiperazine | HCID 61380 | — |
| 反応物 | alpha-(4-Bromophenyl)-3-(tert-butyldimethylsilyloxy)benzyl chloride | HCID 22350043 | — |
| 反応物 | L-Ala-L-Ala diketopiperazine | HCID 131720131 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (2s,5s)-1-(4-Bromo-alpha-(3-(tert-butyldimethylsilyloxy)phenyl)benzyl)-2,5-dimethylpiperazine | HCID 57043709 | 39% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05985880 |
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| 出典データセット | uspto-grants-1999_11 |
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| ORD ID | ord-901068fd391a49e8b2feaf7a44c022d2 |
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| 出典メモ | uspto-grants-1999_11 |
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