戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 72149作成日:2026年10月24日

Triethylamine → [(R)-3-((S)-2-benzyloxycarbonylamino-3-methyl-butyrylamino)-2-hydroxy-propyl]-cyclohexylmethyl-phosphinic acid benzyl ester

https://huagongshe.com/ja/reaction/72149

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物CarbodiimideHCID 160435—
反応物N-Carbobenzoxy-L-valineHCID 726987—
反応物((R)-3-amino-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid benzyl ester hydrochlorideHCID 68622110—
反応物HCID 178418300HCID 178418300—
溶媒DichloromethaneHCID 6344—
生成物[(R)-3-((S)-2-benzyloxycarbonylamino-3-methyl-butyrylamino)-2-hydroxy-propyl]-cyclohexylmethyl-phosphinic acid benzyl esterHCID 6862094226.9%

反応手順

To a solution of N-Cbz-L-valine (1.0 g, 3.98 mmol) dissolved in CH2Cl2 (80 mL) under nitrogen was added hydroxybenzotriazole (0.538 g, 3.98 mmol) and PS-Carbodiimide (2.25 g, 5.17 mmol). After stirring for 10 min, triethylamine (0.665 mL, 4.78 mmol) and ((R)-3-amino-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid benzyl ester hydrochloride (1.44 g, 3.98 mmol) were added. The reaction was stirred for 2 h, then filtered and concentrated in vacuo. The residue was purified by flash chromatography with methanol/dichloromethane on a 35 g RediSep disposable column to give [(R)-3-((S)-2-benzyloxycarbonylamino-3-methyl-butyrylamino)-2-hydroxy-propyl]-cyclohexylmethyl-phosphinic acid benzyl ester (0.60 g, 1.07 mmol) as a white foam. NMR and MS spectra were substantially similar to the product obtained via Method A set forth above.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828974B2
出典データセットuspto-grants-2014_09
ORD IDord-3566b976c00948f68d243c612bfd079f
出典メモuspto-grants-2014_09