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2-(Tributylstannyl)pyridine → 6-Fluoro-3-methoxy-[2,2']bipyridine

HRID 228802
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HRID 228802 반응식
[F:1][C:2]1[N:7]=[C:6](I)[C:5]([O:9][CH3:10])=[CH:4][CH:3]=1.C([Sn](CCCC)(CCCC)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=1)CCC>CN(C)C=O.[Cu]=O>[F:1][C:2]1[N:7]=[C:6]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=2)[C:5]([O:9][CH3:10])=[CH:4][CH:3]=1
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참가 물질

5

반응물 2

HCID 6077842-(Tributylstannyl)pyridineHCID 23078267HCID 23078267, 화합물

생성물 1

HCID 688295916-Fluoro-3-methoxy-[2,2']bipyridine수율 18%

시약·촉매·용매 2

HCID 14829Copper oxide촉매HCID 6228Dimethylformamide용매

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온도
100 °C

실험 절차

6-Fluoro-2-iodo-3-methoxypyridine (84 mg), tetrakistriphenylphosphine palladium (0) (38 mg), and copper(II) oxide (53 mg) were suspended in N,N-dimethylformamide (2 ml). 2-Tributylstannylpyridine (244 mg) was added to the suspension, and the mixture was stirred at 100° C. overnight. The reaction solution was cooled to room temperature. The reaction solution was then filtered, the solvent was removed from the filtrate by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with dichloromethane. The dichloromethane layer was washed with water and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using chloroform-methanol to give 6-fluoro-3-methoxy-[2,2′]bipyridine (12 mg, yield 18%).

후처리

  1. temperatureThe reaction solution was cooled to room temperature
  2. filtrationThe reaction solution was then filtered
  3. customthe solvent was removed from the filtrate by distillation under the reduced pressure
  4. additionWater was then added to the residue
  5. extractionthe mixture was extracted with dichloromethane
  6. washThe dichloromethane layer was washed with water and saturated brine
  7. dry with materialwas dried over anhydrous magnesium sulfate
  8. customThe solvent was removed by distillation under the reduced pressure
  9. customthe residue was purified by thin layer chromatography

출처 및 근거

ORD 기록
ord-87cd9bb304b14f96a297f407fe6aaae9
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07560558B2

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