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HRID 844830作成日:2026年10月26日
(S)-(-)-N-Benzyl-1-phenylethylamine → (S)-3-[2-(4-Acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic Acid (S)-N-Benzyl-alpha-methylbenzylamine Salt
https://huagongshe.com/reaction/844830
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | (S)-(-)-N-Benzyl-1-phenylethylamine | HCID 1268085 | — |
| 反応物 | (+/-)-3-[2-(4-Acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acid | HCID 9827476 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (S)-3-[2-(4-Acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic Acid (S)-N-Benzyl-alpha-methylbenzylamine Salt | HCID 86758013 | 43% |
反応手順
Ethanol (125 g) was added to (+/−)-3-[2-(4-acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acid (11a, 25 g, 85 mmol) and the resulting solution stirred at 20° C. (S)-N-Benzyl-α-methylbenzylamine (21, 22.5 g, 106 mmol) was added to the solution and the resulting mixture allowed to stir at 20° C. for 23 hours. The mixture was filtered and the product washed with ethanol (10 mL) and vacuum dried at ambient temperature to give (S)-3-[2-(4-acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acid (S)-N-benzyl-α-methylbenzylamine salt (22a): 18.6 g (36.8 mmol, 43% yield or 86% of theory); Chiral assay (HPLC): 99.2 area % (S) isomer 23a; mp: 152-154° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06380400B1 |
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| 出典データセット | uspto-grants-2002_04 |
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| ORD ID | ord-a06b05bdbbdc43fe9632c2941295f96a |
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| 出典メモ | uspto-grants-2002_04 |
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