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HRID 596807作成日:2026年10月24日

N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine amide → N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-2-amino-2-methylpropionamide

https://huagongshe.com/ja/reaction/596807

反応式

関与物質

役割名称HCID仕込み量
反応物N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine amideHCID 22796331—
反応物L-methionyl-L-aspartyl-2-amino-2-methylpropionamide hydrochlorideHCID 131710666—
溶媒WaterHCID 962—
生成物N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-2-amino-2-methylpropionamideHCID 131710665—

反応手順

When an equivalent quantity of L-methionyl-L-aspartyl-2-amino-2-methylpropionamide hydrochloride is substituted for the L-methionyl-L-aspartyl-D-alanine amide hydrochloride of Example 6, and the procedure detailed therein substantially repeated, there is obtained N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-2-amino-2-methylpropionamide containing 1/3 mole of water of hydration per mole. This compound is represented by the following formula. ##STR15##Elemental analysis of this compound shows C: 54.45%; H: 6.69%; N: 12.69% and S: 4.96%. Theory is C: 54.36%; H: 6.71%; N: 13.11% and S: 5.00%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04012367
出典データセットuspto-grants-1977_03
ORD IDord-bf8b7d2b172a4c23b3ee148aaba75f04
出典メモuspto-grants-1977_03