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Dimethylformamide → 4-Chloro-2-(2-fluorophenyl)thieno[2,3-d]pyrimidine

HRID 1354293
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HRID 1354293 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[NH:9][C:10](=O)[C:11]2[CH:16]=[CH:15][S:14][C:12]=2[N:13]=1.S(Cl)([Cl:20])=O.CN(C)C=O>C(Cl)(Cl)Cl>[Cl:20][C:10]1[C:11]2[CH:16]=[CH:15][S:14][C:12]=2[N:13]=[C:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[F:1])[N:9]=1
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 211043032-(2-Fluoro-phenyl)-3H-thieno[2,3-d]pyrimidin-4-one

생성물 1

HCID 211043364-Chloro-2-(2-fluorophenyl)thieno[2,3-d]pyrimidine수율 45.3%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

2-(2-Fluoro-phenyl)-3H-thieno[2,3-d]pyrimidin-4-one (900 mg, 3.65 mmole) was dissolved in chloroform and thionyl chloride (0.532 ml, 7.30 mmole) was added to the mixture followed by 1 ml dimethylformamide. Heated the reaction mixture to reflux for 2.5 hours, the cooled mixture was washed with 10% sodium carbonate, dried the chloroform solution over sodium sulfate (anh) and removed solvent. The crude product was chromatographed on silica gel, eluting with chloroform. Upon removal of solvent obtained 438 mg product (yield: 45%).

후처리

  1. temperatureHeated the reaction mixture
  2. temperatureto reflux for 2.5 hours
  3. washthe cooled mixture was washed with 10% sodium carbonate
  4. dry with materialdried the chloroform solution over sodium sulfate (anh)
  5. customremoved solvent
  6. customThe crude product was chromatographed on silica gel
  7. washeluting with chloroform
  8. customUpon removal of solvent

출처 및 근거

ORD 기록
ord-05e905e18cfe408ca7e901b66950d7b5
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07223766B2

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