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HRID 596814作成日:2026年10月27日

N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine amide → N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-N1-propyl-2-amino-2-methylpropionamide

https://huagongshe.com/reaction/596814

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-N1-propyl-2-amino-2-methylpropionamide hydrochloride hydrateHCID 131710669—
生成物N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-N1-propyl-2-amino-2-methylpropionamideHCID 131710668—

反応手順

When an equivalent quantity of L-methionyl-L-aspartyl-N1 -propyl-2-amino-2-methylpropionamide hydrochloride hydrate 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-N1 -propyl-2-amino-2-methylpropionamide hydrated with 2/3 mole of water per mole. Actual elemental analysis shows C: 55.82%; H: 7.21%; N: 12.37% and S: 4.72%. Theoretical elemental analysis is C: 55.79%; H: 7.22%; N: 12.20% and S: 4.66%. This compound is represented by the following formula. ##STR17##

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-5e54c9aa9fb34732b7e0d633c727d277
出典メモuspto-grants-1977_03