5-Fluorouracil → HCID 20525034、化合物

HRID 1702776ノート

反応式

HRID 1702776 の反応式
[CH2:1]([O:3][CH2:4][CH2:5][N:6]=[C:7]=[O:8])[CH3:2].[F:9][C:10]1[C:11](=[O:17])[NH:12][C:13](=[O:16])[NH:14][CH:15]=1>CN(C)C(=O)C.C(OCC)(=O)C>[CH2:1]([O:3][CH2:4][CH2:5][NH:6][C:7]([N:14]1[CH:15]=[C:10]([F:9])[C:11](=[O:17])[NH:12][C:13]1=[O:16])=[O:8])[CH3:2]

参加物

5

反応物 2

HCID 33855-FluorouracilHCID 12017510Ethane, 1-ethoxy-2-isocyanato-

生成物 1

HCID 20525034HCID 20525034、化合物

試薬・触媒・溶媒 2

HCID 8857Ethyl Acetate溶媒HCID 31374Dimethylacetamide溶媒

実験手順

To the above solution of 2-ethoxyethyl isocyanate was added a solution of 5-fluorouracil (2.60 g.) in N,N-dimethylacetamide (20 ml.) at 80° and stirred for further 3 hours at the same temperature. The resultant mixture was diluted with ethyl acetate (200 ml.), washed with saturated sodium chloride aqueous solution (each 30 ml., 2 times), dried over magnesium sulfate, treated with activated charcoal, filtered and evaporated in vacuo. The residue was recrystallized from ethyl acetate to give 1-[N-(2-ethoxyethyl)carbamoyl]-5-fluorouracil (1.82 g.).

後処理

  1. washwashed with saturated sodium chloride aqueous solution (each 30 ml
  2. dry with material, 2 times), dried over magnesium sulfate
  3. additiontreated with activated charcoal
  4. filtrationfiltered
  5. customevaporated in vacuo
  6. customThe residue was recrystallized from ethyl acetate

出典と根拠

ORDレコード
ord-f82239b5cd154925b0365af15a796a6a
出典データセット
uspto-grants-1982_09
特許番号
US04349552

反応ノート

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