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

HRID 228802
ノート
印刷プレビュー

反応式

HRID 228802 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 6077842-(Tributylstannyl)pyridineHCID 23078267HCID 23078267、化合物

生成物 1

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

試薬・触媒・溶媒 2

HCID 14829Copper oxide触媒HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-87cd9bb304b14f96a297f407fe6aaae9
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07560558B2

反応ノート

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