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Triethylamine → 5-Ethenylpyridin-2-amine

HRID 855600
ノート
印刷プレビュー

反応式

HRID 855600 の反応式
[CH:1]([Sn](CCCC)(CCCC)CCCC)=[CH2:2].C(N(CC)CC)C.C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.Br[C:46]1[CH:47]=[CH:48][C:49]([NH2:52])=[N:50][CH:51]=1>C(#N)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH:1]([C:46]1[CH:47]=[CH:48][C:49]([NH2:52])=[N:50][CH:51]=1)=[CH2:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8471TriethylamineHCID 706222-Amino-5-bromopyridineHCID 80271Tri-o-tolylphosphineHCID 81998Tributylvinyltin

生成物 1

HCID 220320805-Ethenylpyridin-2-amine収率 74%

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒
HCID 6342
Acetonitrile
溶媒

実験手順

Vinyltributyltin (13 mL, 44.6 mmol), palladium(II) acetate (0.45 g, 2.1 mmol), triethylamine (12.4 mL, 89.1 mmol) and tri-(o-tolyl)phosphine (3.69 g, 12.15 mmol) were added to a solution of 5-bromopyridin-2-amine (7.0 g, 40.5 mmol) in acetonitrile (70 mL) and the reaction mixture refluxed for 18 hours. The reaction mixture was washed with 2M sodium carbonate solution (80 mL), the organics separated, dried over magnesium sulphate, filtered and concentrated in vacuo. The crude product was purified by column chromatography on silica gel using methanol:dichloromethane 3:97 to yield 3.6 g of product. This residue was dissolved in dichloromethane and washed with aqueous solutions of potassium fluoride and then sodium hydrogencarbonate. The organic solution was dried over magnesium sulphate, filtered and concentrated in vacuo to yield 1.9 g of final product.

後処理

  1. temperaturethe reaction mixture refluxed for 18 hours
  2. washThe reaction mixture was washed with 2M sodium carbonate solution (80 mL)
  3. dry with materialthe organics separated, dried over magnesium sulphate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe crude product was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-1748d3059dbe49f992c3a7d8243c37fb
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07262192B2

反応ノート

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