Hydrochloric Acid → 8-Guanidino-3-hydroxyoctanamide hydrochloride

HRID 462905

반응식

HRID 462905 반응식
[ClH:1].[NH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH:8]([OH:13])[CH2:9][C:10]([NH2:12])=[O:11].S(O)(O)(=O)=O.CS[C:21](=[NH:23])[NH2:22].CSC(=N)N.Cl>[OH-].[Na+]>[ClH:1].[NH:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH:8]([OH:13])[CH2:9][C:10]([NH2:12])=[O:11])[C:21]([NH2:23])=[NH:22]

참가 물질

5

실험 절차

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.

후처리

  1. customevaporated to dryness
  2. dissolutiondissolved in 5 ml of 1M saline
  3. washthe 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)
  4. customevaporated to dryness
  5. extractionextracted three times with 10 ml of methanol
  6. washeluted with methanol to effect
  7. customevaporated to dryness

출처 및 근거

ORD 기록
ord-17387d8a505046deb755ca3a22d61c2b
출처 데이터셋
uspto-grants-1985_05
특허 번호
US04518532

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