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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

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-(-)-N-Benzyl-1-phenylethylamineHCID 1268085—
反応物(+/-)-3-[2-(4-Acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acidHCID 9827476—
溶媒EthanolHCID 702—
生成物(S)-3-[2-(4-Acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic Acid (S)-N-Benzyl-alpha-methylbenzylamine SaltHCID 8675801343%

反応条件

温度20 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06380400B1
出典データセットuspto-grants-2002_04
ORD IDord-a06b05bdbbdc43fe9632c2941295f96a
出典メモuspto-grants-2002_04