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HRID 4981作成日:2026年10月25日

Hydrochloric Acid → Ac-Ala-Lys(Boc)-OH

https://huagongshe.com/reaction/4981

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物N-HydroxysuccinimideHCID 80170—
反応物N-Acetyl-L-alanineHCID 88064—
反応物(2S)-2-amino-6-(((tert-butoxy)carbonyl)amino)hexanoic acidHCID 2733283—
溶媒1,4-DioxaneHCID 31275—
生成物Ac-Ala-Lys(Boc)-OHHCID 131717743—

反応手順

Ac-Ala-Lys(Boc)-OH was prepared by coupling the N-hydroxysuccinimide ester of Ac-Ala-OH, prepared by the method of Anderson et al., J. Am. Chem. Soc. 86: 1839, (1964), to H-Lys(Boc)-OH. The N-hydroxy-succinimide of Ac-Ala-OH (6.25 g, 27.4 mmoles) was dissolved in 30 mL of dioxane and was added to a solution of H-Lys(Boc)-OH (7.50 g, 30.4 mmoles) dissolved in a solution consisting of 30 mL of 1.0N sodium hydroxide and triethylamine (2.12 mL, 15.0 mmoles). The reaction mixture was stirred overnight, then acidified with hydrochloric acid. Sufficient dry sodium chloride to nearly saturate the solution was added. The product was extracted into ethyl acetate and it was washed with 0.2N hydrochloric acid prepared in saturated aqueous sodium chloride. The organic phase was dried over anhydrous sodium sulfate and filtered. Solvent was removed by evaporation. The product was crystallized from ethyl acetate:hexane to yield 7.3 g (mp 86°-89°).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242904
出典データセットuspto-grants-1993_09
ORD IDord-408c8484fe124834b5520e846e9adf68
出典メモuspto-grants-1993_09