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Phosphorus oxychloride → HCID 70454969、化合物

HRID 2418681
ノート
印刷プレビュー

反応式

HRID 2418681 の反応式
[C:1]([NH:4][CH2:5][C:6]1[NH:7][C:8](=[O:13])[NH:9][C:10](=O)[CH:11]=1)(=O)[CH3:2].P(Cl)(Cl)([Cl:16])=O>>[Cl:16][C:10]1[CH:11]=[C:6]2[CH:5]=[N:4][CH:1]([CH3:2])[N:7]2[C:8](=[O:13])[N:9]=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 24813Phosphorus oxychlorideHCID 21793940N-[(2,6-Dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)methyl]acetamide

生成物 1

HCID 70454969HCID 70454969、化合物

実験手順

A suspension of 6.63 g (36.2 mmole) of 4-acetylaminomethylpyrimidine-2,6-dione in 250 ml of phosphorous oxychloride was heated at reflux for 20 hours, and was cooled and evaporated. The residue was added to about 700 ml of cold saturated sodium bicarbonate solution. To the resulting mixture was added 200 ml of chloroform and enough solid sodium bicarbonate to neutralize the mixture. The solid was separated by filtration, washed with water and ethanol, and recrystallized from ethanol to provide yellow solid 7-chloro-3-methylimidazo[1,5-c]pyrimidin-5-one, m.p. 239° C. (dec.). Analysis: Calculated for C7H6ClN3O; %C, 45.8; %H, 3.3; %N, 22.9; Found; %C, 45.8; %H, 3.1; %N, 22.8.

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 20 hours
  3. temperature
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
was cooled
  • customevaporated
  • additionThe residue was added to about 700 ml of cold saturated sodium bicarbonate solution
  • additionTo the resulting mixture was added 200 ml of chloroform and enough solid sodium bicarbonate
  • customThe solid was separated by filtration
  • washwashed with water and ethanol
  • customrecrystallized from ethanol
  • 出典と根拠

    ORDレコード
    ord-f1598504103e4ae78d30d391352fbc84
    出典データセット
    uspto-grants-1984_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04473570

    反応ノート

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