関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Bis(S-methylisothiouronium) sulfate | HCID 13347 | — |
| 反応物 | 8-Amino-3-hydroxyoctanamide hydrochloride | HCID 22149892 | — |
| 溶媒 | Sodium Hydroxide | HCID 14798 | — |
| 生成物 | 8-Guanidino-3-hydroxyoctanamide hydrochloride | HCID 178479437 | 113.3% |
反応手順
To a solution of 670 mg of 8-amino-3-hydroxyoctanamide hydrochloride in 8 ml of 1N aqueous sodium hydroxide solution, was added 668 mg (2.4 mmoles) of S-methylisothiourea hemisulfate. The mixture was stirred overnight at room temperature. The reaction mixture was adjusted to pH 6 with 1N hydrochloric acid, evaporated to dryness and dissolved in 5 ml of 1M saline. The solution was passed through a column of 160 ml of Diaion® HP-20 (Mitsubishi Chemical Co.) and the column was eluted successively with 400 ml of 1M saline, 400 ml of 0.8M saline and 800 ml of 0.6M saline (15 g fraction size). Fractions No. 41 to No. 87 were combined, evaporated to dryness and extracted three times with 10 ml of methanol. The methanol layer was passed through a column of 300 ml of Sephadex® LH-20 and eluted with methanol to effect desalting (7 ml fraction size). Fractions No. 25 to 35 were combined and evaporated to dryness to obtain 687 mg (85% yield) of 8-guanidino-3-hydroxyoctanamide hydrochloride.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04518532 |
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| 出典データセット | uspto-grants-1985_05 |
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| ORD ID | ord-17387d8a505046deb755ca3a22d61c2b |
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| 出典メモ | uspto-grants-1985_05 |
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