Diethyl Ether → 4-Chloro-6-(1-ethoxyvinyl)pyrimidine

HRID 2401187ノート

反応式

HRID 2401187 の反応式
[Cl:1][C:2]1[CH:7]=[C:6](Cl)[N:5]=[CH:4][N:3]=1.C([Sn](CCCC)(CCCC)[C:14]([O:16][CH2:17][CH3:18])=[CH2:15])CCC.[F-].[K+].C(OCC)C>CN(C=O)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[C:6]([C:14]([O:16][CH2:17][CH3:18])=[CH2:15])[N:5]=[CH:4][N:3]=1

参加物

7

反応条件

温度
80 °C

実験手順

4,6-Dichloropyrimidine (1.0 g, 6.71 mmol), bis(triphenylphosphine)palladium(II) chloride (0.094 g, 0.134 mmol) and tributyl[1-(ethyloxy)ethenyl]stannane (2.449 mL, 7.25 mmol) were added together in DMF (25 mL) and the resulting mixture was heated at 80° C. under argon for 18 hours. The reaction mixture was allowed to cool to room temperature and poured into an aqueous solution of potassium fluoride (5.7 g in 57 mL water). Diethyl ether (80 mL) was added and the solid was filtered, washed with diethyl ether (×2) and discarded. The filtrate was separated and the organic layer was washed with water, dried under magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography (Biotage SP4) eluting with a gradient of 0-20% ethyl acetate and iso-hexane. Product containing fractions were combined and evaporated under reduced pressure to give the title compound as a white solid (564 mg);

後処理

  1. temperatureto cool to room temperature
  2. filtrationthe solid was filtered
  3. washwashed with diethyl ether (×2)
  4. customThe filtrate was separated
  5. washthe organic layer was washed with water
  6. customdried under magnesium sulfate
  7. customevaporated under reduced pressure
  8. customThe residue was purified by column chromatography (Biotage SP4)
  9. washeluting with a gradient of 0-20% ethyl acetate and iso-hexane
  10. additionProduct containing fractions
  11. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-844f1176d3df4a2b9213078e8191a284
出典データセット
uspto-grants-2014_08
特許番号
US08796283B2

反応ノート

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