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HRID 436955作成日:2026年10月25日

4-Methylmorpholine → N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanine benzyl ester

https://huagongshe.com/reaction/436955

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物HCID 13273165HCID 13273165—
反応物Benzyl glycyl-L-alaninate hydrochlorideHCID 53328828—
溶媒DichloromethaneHCID 6344—
生成物N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanine benzyl esterHCID 53750798—

反応手順

A solution of 17.6 parts N-t-butoxycarbonyl-L-tyrosine 2,4,5-trichlorophenyl ester, 9.0 parts glycyl-L-alanine benzyl ester hydrochloride and 1.2 parts N-methylmorpholine in 200 parts methylene chloride is stirred for 16 hours at room temperature. Removal of the solvent under reduced pressure affords a crude product which is purified by low pressure column chromatography to give N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanine benzyl ester. The purified material is dissolved in 400 parts methanol. Then, 0.4 part palladium black metal catalyst is added and the mixture shaken with hydrogen at atmospheric pressure and room temperature for about 5 hours. The catalyst is removed by filtration, and the solvent is removed by evaporation under reduced pressure. The resulting material is purified by low-pressure chromatography to give N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanine. This compound is represented by the following formula

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04028319
出典データセットuspto-grants-1977_06
ORD IDord-7dd09a1cefae4b53a49903cf89014486
出典メモuspto-grants-1977_06