ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

5-Fluorouracil → HCID 12812862、化合物

HRID 1702787
ノート
印刷プレビュー

反応式

HRID 1702787 の反応式
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][N:8]=[C:9]=[O:10])=[CH:3][CH:2]=1.[F:11][C:12]1[C:13](=[O:19])[NH:14][C:15](=[O:18])[NH:16][CH:17]=1>>[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][NH:8][C:9]([N:16]2[CH:17]=[C:12]([F:11])[C:13](=[O:19])[NH:14][C:15]2=[O:18])=[O:10])=[CH:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 33855-FluorouracilHCID 204582734-(Isocyanatomethyl)pyridine

生成物 1

HCID 12812862HCID 12812862、化合物

実験手順

To the above solution of 4-pyridylmethyl isocyanate was added 5-fluorouracil (2.60 g.) at 80° C. and stirred for 4 hours at the same temperature. The resultant mixture was evaporated in vacuo. The residue was washed with diethyl ether (3 times) and crystallized. The crystals were filtered and washed with a small amount of ethanol. To the washed crystals a small amount of pyridine was added, and the mixture was warmed to be dissolved and cooled to be recrystallized. The crystals were washed successively with ethyl acetate and diethyl ether to give 1-[N-(4-pyridylmethyl)carbamoyl]-5-fluorouracil (1.75 g.)

後処理

  1. customThe resultant mixture was evaporated in vacuo
  2. washThe residue was washed with diethyl ether (3 times)
  3. customcrystallized
  4. filtrationThe crystals were filtered
  • washwashed with a small amount of ethanol
  • additionTo the washed crystals a small amount of pyridine was added
  • temperaturethe mixture was warmed
  • dissolutionto be dissolved
  • temperaturecooled
  • customto be recrystallized
  • washThe crystals were washed successively with ethyl acetate and diethyl ether
  • 出典と根拠

    ORDレコード
    ord-f856788c31b34ea696eca4220a64e135
    出典データセット
    uspto-grants-1982_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04349552

    反応ノート

    読み込み中…

    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