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HRID 5727作成日:2026年10月25日

1-Phenylpiperazine → 1-(N-Benzyloxycarbonyltyrosyl)-4-phenylpiperazine

https://huagongshe.com/reaction/5727

反応式

関与物質

役割名称HCID仕込み量
反応物1-PhenylpiperazineHCID 7096—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物N-benzyloxycarbonyl-l-tyrosineHCID 712438—
溶媒DichloromethaneHCID 6344—
生成物1-(N-Benzyloxycarbonyltyrosyl)-4-phenylpiperazineHCID 5446385658.6%

反応手順

12.3 g of N-benzyloxycarbonyltyrosine and 6.6 g of N-phenylpiperazine were dissolved in 150 ml of methylene chloride, and to the solution was added 8.4 g of DCC, and the mixture was stirred at a room temperature for 5 hours. Precipitated insoluble matter was filtered off and the filtrate was concentrated under a reduced pressure, and resulting residue was applied to a silica gel column and eluted with hexane/ethyl acetate (1:1 to 1:2) to obtain 10.5 g of the title compound in a colorless amorphous form.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05245034
出典データセットuspto-grants-1993_09
ORD IDord-6fb0cb4113fb499eb4dfc30867774f34
出典メモuspto-grants-1993_09