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Dimethylformamide → HCID 22735171、化合物

HRID 50572
ノート
印刷プレビュー

反応式

HRID 50572 の反応式
[CH:1]1[CH:6]=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=C[CH:2]=1.Br[C:21]1[CH:22]=[N:23][CH:24]=[C:25]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][N:28]=2)[CH:26]=1.CN(C=[O:37])C>C(OCC)(=O)C.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[N:28]1[CH:29]=[CH:30][CH:31]=[CH:32][C:27]=1[C:25]1[CH:26]=[C:21](/[CH:2]=[CH:1]/[CH:6]=[O:37])[CH:22]=[N:23][CH:24]=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

6

反応物 3

HCID 6228DimethylformamideHCID 11776TriphenylphosphineHCID 227351815'-Bromo-2,3'-bipyridine

生成物 1

HCID 22735171HCID 22735171、化合物

試薬・触媒・溶媒 2

HCID 9811564Bis(dibenzylideneacetone)palladium触媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
25 °C

実験手順

A mixture of Pd2(dba)3 (36 mg, 0.04 mmol) and PPh3 (triphenylphosphine) in DMF (degassed, 2.0 mL) was allowed to stir for 5 min. at 25° C. 1,1′-Diethyl 3-(tributyltin)-propenylacetal (0.44 g, 1.27 mmol) and 3-bromo-5-(2-pyridinyl)-pyridine (100 mg, 0.42 mmol) were added and the resulting mixture was warmed to 80° C. After 18 h, the reaction mixture was allowed to cool to 25° C., diluted with ethyl acetate (100 mL), washed with brine (1×50 mL) and concentrated in vacuo. The residue was dissolved in 2N aqueous HCl (2.0 mL) and allowed to stir for 30 min. The reaction mixture was neutralized by the addition of sodium bicarbonate until the pH ˜7, diluted with ethyl acetate (100 mL), washed with brine (1×50 mL), and concentrated in vacuo. Purification by flash chromatography (0-50% EtOAc/hexanes) afforded the title compound (10 mg) as a white solid. MS 211 (M+H)+.

後処理

  1. temperaturethe resulting mixture was warmed to 80° C
  2. waitAfter 18 h
  3. temperatureto cool to 25° C.
  4. washwashed with brine (1×50 mL)
  5. concentrationconcentrated in vacuo
  6. dissolutionThe residue was dissolved in 2N aqueous HCl (2.0 mL)
  7. stirringto stir for 30 min
  8. additionThe reaction mixture was neutralized by the addition of sodium bicarbonate until the pH ˜7
  9. additiondiluted with ethyl acetate (100 mL)
  10. washwashed with brine (1×50 mL)
  11. concentrationconcentrated in vacuo
  12. customPurification by flash chromatography (0-50% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-ee06eb1885d14711ab40a55ff4ced6ab
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06713455B2

反応ノート

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