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Sodium Methoxide → 4-(4-Bromophenyl)-2-(2,6-difluorophenyl)-3-methoxypyrimidine

HRID 2119789
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인쇄 미리보기

반응식

HRID 2119789 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9](Cl)[CH:10]([C:14]3[C:19]([F:20])=[CH:18][CH:17]=[CH:16][C:15]=3[F:21])[N:11]=[CH:12][CH:13]=2)=[CH:4][CH:3]=1.[CH3:23][O-:24].[Na+]>CO>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]([O:24][CH3:23])[CH:10]([C:14]3[C:19]([F:20])=[CH:18][CH:17]=[CH:16][C:15]=3[F:21])[N:11]=[CH:12][CH:13]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 23443407HCID 23443407, 화합물

생성물 1

HCID 234434084-(4-Bromophenyl)-2-(2,6-difluorophenyl)-3-methoxypyrimidine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

6 g of 4-(4-bromophenyl)-2-(2,6-difluorophenyl)-3-chloropyrimidine, 60 ml of methanol and 3.3 g of methanolic sodium methanolate solution (30%) are boiled under reflux for 24 hours, concentrated by evaporation, and the residue taken up in ethyl acetate and the organic phase washed with water. After drying with magnesium sulfate, filtering and concentrating, the title compound is obtained with a melting point of 104-106° C. (compound 3.350).

후처리

  1. temperatureunder reflux for 24 hours
  2. concentrationconcentrated by evaporation
  3. washthe organic phase washed with water
  4. dry with materialAfter drying with magnesium sulfate
  5. filtrationfiltering
  6. concentrationconcentrating

출처 및 근거

ORD 기록
ord-c8b2489972b1447eb848d4c112719d8a
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06686469B2

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