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Phosphorus oxychloride → HCID 19967110, 화합물

HRID 976329
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HRID 976329 반응식
[N:1]1([CH2:6][C:7]2[CH:8]=[C:9]3[C:14](=[CH:15][CH:16]=2)[NH:13][C:12](=O)[CH:11]=[C:10]3[CH3:18])[CH:5]=[CH:4][N:3]=[CH:2]1.P(Cl)(Cl)([Cl:21])=O>>[Cl:21][C:12]1[CH:11]=[C:10]([CH3:18])[C:9]2[C:14](=[CH:15][CH:16]=[C:7]([CH2:6][N:1]3[CH:5]=[CH:4][N:3]=[CH:2]3)[CH:8]=2)[N:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 19967123HCID 19967123, 화합물

생성물 1

HCID 19967110HCID 19967110, 화합물수율 12.5%

실험 절차

A solution of 13 parts of 6-(1H-imidazol-1-ylmethyl)-4-methyl-2(1H)-quinolinone in 55 parts of phosphoryl chloride was stirred for 1 hour at room temperature. After evaporation, the residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of acetonitrile and 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.75 parts (12.5%) of 2-chloro-6-(1H-imidazol-1-ylmethyl)-4-methylquinoline; mp. 120.6° C. (compound 34).

후처리

  1. customAfter evaporation
  2. customthe residue was purified by column chromatography over silica gel using
  3. addition
a mixture of trichloromethane and methanol (95:5 by volume) as eluent
  • customThe pure fractions were collected
  • customthe eluent was evaporated
  • customThe residue was crystallized from a mixture of acetonitrile and 2,2'-oxybispropane
  • filtrationThe product was filtered off
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-64368920388a4b04add527b2f9ae42f9
    출처 데이터셋
    uspto-grants-1997_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05612354

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