戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 430804作成日:2026年10月25日

1-Phenylcyclopentanecarboxylic acid → (s)-1-Phenyl-cyclopentanecarboxylic acid [2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-amide

https://huagongshe.com/reaction/430804

反応式

関与物質

役割名称HCID仕込み量
反応物1-Phenylcyclopentanecarboxylic acidHCID 66167—
反応物DiisopropylethylamineHCID 81531—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
反応物(S)-2-amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamideHCID 15517727—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物(s)-1-Phenyl-cyclopentanecarboxylic acid [2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-amideHCID 989212445%

反応条件

温度0 °C

反応手順

1-Phenyl-1-cyclopentanecarboxylic acid (0.171 g, 0.899 mmol) was dissolved in dry DMF (3 mL) under a nitrogen atmosphere and cooled to 0° C. in an ice-water bath. To this solution were added in succession N,N-diisopropylethylamine (0.310 mL, 1.80 mmol) and solid O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.341 g, 0.899 mmol, Novabiochem, La Jolla, Calif.). The resulting reaction mixture was stirred at 0° C. for 30 minutes, (S)-2-Amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide (0.293 g, 0.899 mmol) was then added. After an additional 60 minutes stirring at 0° C., the reaction mixture was mixed with 60 mL of diethyl ether. The resulting mixture was successively washed with 5% aqueous HCl solution, brine, saturated aqueous NaHCO3 solution and brine, and was dried over Na2SO4. The solution was concentrated in vacuo, and an oil was obtained. The crude residue was purified by chromatography (silica gel, 60% ether in hexanes) to give the title compound as a white foam (0.20 g, 45%); mp 40-50° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06323243B1
出典データセットuspto-grants-2001_11
ORD IDord-13f94147e9424f0caa6371d873033357
出典メモuspto-grants-2001_11