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

HRID 2413746
ノート
印刷プレビュー

反応式

HRID 2413746 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 887MethanolHCID 20155477HCID 20155477、化合物

生成物 1

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

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

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.

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
  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

出典と根拠

ORDレコード
ord-01c509f2df684aee922a55c02f0bda7b
出典データセット
uspto-grants-1988_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04719222

反応ノート

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