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HRID 55381作成日:2026年10月25日

Ethyl beta-[[3-[[[4(aminoiminomethyl)phenyl]-amino]thiocarbonyl]aminopropanoyl]amino]propanoate → beta-[[3-[[[4(Aminoiminomethyl)phenyl]amino]-thiocarbonyl]aminopropanoyl]amino]propanoic acid

https://huagongshe.com/reaction/55381

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl beta-[[3-[[[4(aminoiminomethyl)phenyl]-amino]thiocarbonyl]aminopropanoyl]amino]propanoateHCID 86747885—
溶媒Lithium hydroxide methanolHCID 23717829—
生成物beta-[[3-[[[4(Aminoiminomethyl)phenyl]amino]-thiocarbonyl]aminopropanoyl]amino]propanoic acidHCID 86747884—

反応手順

Ethyl β-[[3-[[[4(aminoiminomethyl)phenyl]-amino]thiocarbonyl]aminopropanoyl]amino]propanoate (65 mg; 0.18 mmoles) was treated in 1N lithium hydroxide/methanol (20 ml; 1:1) for 10 min. Methanol was evaporated and the pH of the remaining mixture was adjusted to 5 with 50% acetic acid. The mixture was then purified by HPLC using a linear gradient of acetonitrile/water/0.05% trifluoro-acetic acid (0-20% acetonitrile in 30 min). Yield: 51 mg (85%). FAB-MS: MH+ =338.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624956
出典データセットuspto-grants-1997_04
ORD IDord-df0d4d5dee82469090cced0792a7e844
出典メモuspto-grants-1997_04