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HRID 1765647作成日:2026年10月25日

Ethanol → tert-Butyl 2-(3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)butanoate

https://huagongshe.com/reaction/1765647

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物DiisopropylamineHCID 7912—
反応物tert-Butyl(2R)-2-((3R)-3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)propanoateHCID 69222335—
触媒PalladiumHCID 23938—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl 2-(3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)butanoateHCID 22017281—

反応手順

A mixture of Intermediate 112 [Mixture 1] (0.051 g), 10% palladium on carbon (0.01 g) and ethanol (5 ml) was stirred under an atmosphere of hydrogen for 18 h. The reaction mixture was filtered through Celite™ and the filtrate was concentrated under reduced pressure to give a yellow gum. The gum (0.034 g) in DCM (2 ml) was treated with 6-chloronaphthylsulphonyl chloride1 (0.04 g) and N,N-diisopropylamine (0.073 ml) and stirred at room temperature for 24 h. The mixture was washed with water and concentrated under reduced pressure to yield an oil which was partially purified using SPE (silica, eluting with cyclohexane:ethyl acetate 1:1) to give the title compound (0.043 g) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07226929B2
出典データセットuspto-grants-2007_06
ORD IDord-f0a5a2f7defc4798b831fb93112ca5ed
出典メモuspto-grants-2007_06