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HRID 632562作成日:2026年10月24日

Ethyl Acetate → 1-cyclopentyl N-[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]-L-leucinate

https://huagongshe.com/ja/reaction/632562

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Tert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物L-leucine cyclopentyl ester tosylateHCID 86633653—
溶媒1,1-DichloroethaneHCID 6365—
生成物1-cyclopentyl N-[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]-L-leucinateHCID 86686416—

反応手順

To a solution of N-tert-butoxycarbonyl-3-pyrrolidinone (0.382 g, 4.76 mmol) in dichloroethane (20 mL) was added L-leucine cyclopentyl ester tosylate (1.96 g, 5.3 mmol) and sodium triacetoxyborohydride (2.65 g, 12.5 mmol). The mixture was stirred at room temperature for 3 hours, then poured into ethyl acetate (150 mL) and quenched with saturated ammonium chloride solution (50 mL) and washed with saturated sodium hydrogen carbonate solution (3 times 30 mL). The organic extracts were dried (MgSO4), concentrated and purified by flash column chromatography (7:3 ethyl acetate:heptane) to yield the desired product. LC/MS: m/z 369.25 [M+H]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09321718B2
出典データセットuspto-grants-2016_04
ORD IDord-6da453aad4f84aac847932ee8559d33c
出典メモuspto-grants-2016_04