Citric Acid → (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acid

HRID 427364

반응식

HRID 427364 반응식
[NH:1]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][OH:4].[H-].[Na+].CI.[C:19](O)(=O)CC(CC(O)=O)(C(O)=O)O>CN(C=O)C>[CH3:12][C:11]([O:10][C:8]([NH:1][C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][O:4][CH3:19])=[O:9])([CH3:14])[CH3:13]

참가 물질

6

실험 절차

In a DMF solution containing 2.00 g of Boc-Ser-OH, 0.86 g of sodium hydride (60% oily suspension) was added under ice cooling and the resultant mixture was stirred for 30 min. To the resultant solution, 0.72 ml of methyl iodide was added and the resultant solution was stirred for 3 hr. The reaction mixture was neutralized with citric acid and evaporated under reduced pressure. The obtained residue was redissolved in ethyl acetate, and the solution was washed with 5% aqueous citric acid solution and saturated aqueous sodium chloride solution. successively, and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure. The residue was subjected to a silica gel column chromatography (chloroform:methanol=10:1) and crystallized as its DCHA salt from n-hexane to give 0.79 g of the title compound.

후처리

  1. additionwas added under ice cooling
  2. customevaporated under reduced pressure
  3. dissolutionThe obtained residue was redissolved in ethyl acetate
  4. washthe solution was washed with 5% aqueous citric acid solution and saturated aqueous sodium chloride solution
  5. dry with materialsuccessively, and dried over anhydrous sodium sulfate
  6. customThe dried solution was evaporated under reduced pressure
  7. customcrystallized as its DCHA salt from n-hexane

출처 및 근거

ORD 기록
ord-896f4f68ddd74fc385c1ace3d6b70b1f
출처 데이터셋
uspto-grants-2001_11
특허 번호
US06313094B1

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