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Dimethylformamide → HCID 22735171, Verbindung

HRID 50572
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 50572
[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
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

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

Produkt 1

HCID 22735171HCID 22735171, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 9811564Bis(dibenzylideneacetone)palladiumKatalysator
HCID 8857
Ethyl Acetate
Lösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

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)+.

Aufarbeitung

  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)

Quellen und Nachweise

ORD-Eintrag
ord-ee06eb1885d14711ab40a55ff4ced6ab
Quelldatensatz
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06713455B2

Notizen zur Reaktion

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