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Phosphorus oxychloride → 7-Chloro-5-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine

HRID 1447898
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반응식

HRID 1447898 반응식
O[C:2]1[N:7]2[N:8]=[CH:9][CH:10]=[C:6]2[N:5]=[C:4]([C:11]2[CH:12]=[C:13]([C:17]([F:20])([F:19])[F:18])[CH:14]=[CH:15][CH:16]=2)[CH:3]=1.P(Cl)(Cl)([Cl:23])=O>>[Cl:23][C:2]1[N:7]2[N:8]=[CH:9][CH:10]=[C:6]2[N:5]=[C:4]([C:11]2[CH:12]=[C:13]([C:17]([F:20])([F:19])[F:18])[CH:14]=[CH:15][CH:16]=2)[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178515578HCID 178515578, 화합물

생성물 1

HCID 233298597-Chloro-5-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine

실험 절차

A mixture of 1.75 g. of 7-hydroxy-5-(α,α,α-trifluoro-m-tolyl) pyrazolo[1,5-a]pyrimidine and 15 ml. of phosphorus oxychloride is refluxed for 2 hours. After evaporation at reduced pressure, ice is added to the residue and the desired compound is extracted with methylene chloride. After washing the organic layer with a saturated saline solution and drying with solid anhydrous sodium sulfate, evaporation gives the desired compound, m.p. 137°-139° C.

후처리

  1. additionA mixture of 1.75 g
  2. customAfter evaporation at reduced pressure, ice
  3. additionis added to the residue
  4. extractionthe desired compound is extracted with methylene chloride
  • washAfter washing the organic layer with a saturated saline solution
  • dry with materialdrying with solid anhydrous sodium sulfate, evaporation
  • 출처 및 근거

    ORD 기록
    ord-b18d94dc182e4920a205febb1884b246
    출처 데이터셋
    uspto-grants-1979_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04178449

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