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Phosphorus oxychloride → HCID 70454969, 화합물

HRID 2418681
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HRID 2418681 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 21793940N-[(2,6-Dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)methyl]acetamide

생성물 1

HCID 70454969HCID 70454969, 화합물

실험 절차

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.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 20 hours
  3. temperature
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
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
  • 출처 및 근거

    ORD 기록
    ord-f1598504103e4ae78d30d391352fbc84
    출처 데이터셋
    uspto-grants-1984_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04473570

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