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HRID 2245435作成日:2026年10月25日

tert-butyl N-(2-oxoethyl)carbamate → 1-(1,1-Dimethylethyl) 3-ethyl 4-[2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)ethyl]-1,3-piperazinedicarboxylate

https://huagongshe.com/reaction/2245435

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N-(2-oxoethyl)carbamateHCID 4247255—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-tert-Butyl 3-ethyl piperazine-1,3-dicarboxylateHCID 11402671—
溶媒1,1-DichloroethaneHCID 6365—
生成物1-(1,1-Dimethylethyl) 3-ethyl 4-[2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)ethyl]-1,3-piperazinedicarboxylateHCID 59215848—

反応手順

To a solution of 1-(1,1-dimethylethyl) 3-ethyl 1,3-piperazinedicarboxylate [EP1486498, 2004] (2.023 g, 8.28 mmol) in 10 mL of dichloroethane was added a solution of N-boc-2-aminoacetaldehyde (1.87 g, 12.42 mmol) in 20 mL of dichloroethane. The solution was stirred at room temperature and under nitrogen atmosphere for 30 min. Sodium triacetoxyborohydride (3.32 g, 16.56 mmol) was then added and the reaction kept at room temperature overnight. The product was isolated on a SCX cartridge. 2.492 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07683056B2
出典データセットuspto-grants-2010_03
ORD IDord-8e27253963df46479d7f427cb53c4224
出典メモuspto-grants-2010_03