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Methanol → HCID 178499130, 화합물

HRID 2053095
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HRID 2053095 반응식
S(Cl)(Cl)=[O:2].C([O:12][C:13]1[CH:18]=[C:17]([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:28])([F:27])[F:26])[CH:20]=2)[N:16]=[C:15]([C:29]#N)[N:14]=1)C1C=CC=CC=1.[CH3:31][OH:32]>>[CH3:31][O:32][C:29]([C:15]1[N:14]=[C:13]([OH:12])[CH:18]=[C:17]([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:28])([F:27])[F:26])[CH:20]=2)[N:16]=1)=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 588780594-Benzyloxy-6-(3-trifluoromethyl-phenyl)-pyrimidine-2-carbonitrile

생성물 1

HCID 178499130HCID 178499130, 화합물

실험 절차

To methanol (10 ml) at 0° C. was added thionyl chloride (500 ul). The mixture was stirred for 30 minutes then 4-benzyloxy-6-(3-trifluoromethyl-phenyl)-pyrimidine-2-carbonitrile (300 mg) was added and the reaction was heated to reflux for five hours. Solvent was evaporated under reduced pressure to yield crude product. Purification of the resulting residue by flash chromatography on silica afforded product 4-hydroxy-6-(3-trifluoromethylphenyl)-pyrimidine-2-carboxylic acid methyl ester (104 mg).

후처리

temperature
the reaction was heated
  • temperatureto reflux for five hours
  • customSolvent was evaporated under reduced pressure
  • customto yield crude product
  • customPurification of the resulting residue by flash chromatography on silica afforded product 4-hydroxy-6-(3-trifluoromethylphenyl)-pyrimidine-2-carboxylic acid methyl ester (104 mg)
  • 출처 및 근거

    ORD 기록
    ord-88029350f9954a2381d330aee223a8f6
    출처 데이터셋
    uspto-grants-2008_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07326715B2

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