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Methanol → N-(2-Amino-2-oxoethyl)-2,2-dimethyl-5-oxo-1-imidazolidineacetamide

HRID 2413746
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HRID 2413746 반응식
[C:1](O)(=O)[CH3:2].[NH2:5][CH2:6][C:7]([NH:9][CH2:10][C:11]([NH:13][CH2:14][C:15]([NH2:17])=[O:16])=[O:12])=[O:8].[CH3:18]O>CC(C)=O>[CH3:18][C:1]1([CH3:2])[NH:5][CH2:6][C:7](=[O:8])[N:9]1[CH2:10][C:11]([NH:13][CH2:14][C:15]([NH2:17])=[O:16])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 887MethanolHCID 20155477HCID 20155477, 화합물

생성물 1

HCID 54125798N-(2-Amino-2-oxoethyl)-2,2-dimethyl-5-oxo-1-imidazolidineacetamide

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution of glycylglycylglycinamide acetate (800 mg) in methanol (8 ml) and acetone (15 ml), Amberlite IRA-68 resin (2 ml) was added. The suspension was stirred at room temperature for 1 hour, then the resin was filtered off and the solution was evaporated under reduced pressure. The residue was suspended in acetone and stirred at room temperature overnight. The precipitate was collected and crystallized from ethyl acetate, to give the title compound, as a white powder, m.p. 102°-105° C. dec.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. filtrationthe resin was filtered off
  2. customthe solution was evaporated under reduced pressure
  3. stirringstirred at room temperature overnight
  4. customThe precipitate was collected
  5. customcrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-01c509f2df684aee922a55c02f0bda7b
출처 데이터셋
uspto-grants-1988_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04719222

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