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Ethyl beta-[[3-[[[4(aminoiminomethyl)phenyl]-amino]thiocarbonyl]aminopropanoyl]amino]propanoate → beta-[[3-[[[4(Aminoiminomethyl)phenyl]amino]-thiocarbonyl]aminopropanoyl]amino]propanoic acid
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]propanoate | HCID 86747885 | — |
| 溶媒 | Lithium hydroxide methanol | HCID 23717829 | — |
| 生成物 | beta-[[3-[[[4(Aminoiminomethyl)phenyl]amino]-thiocarbonyl]aminopropanoyl]amino]propanoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05624956 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-df0d4d5dee82469090cced0792a7e844 |
| 出典メモ | uspto-grants-1997_04 |