Sodium Carbonate → 2-Chloro-4-(2,3,4-trimethoxyphenyl)pyrimidine

HRID 497026Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 497026
[Cl:1][C:2]1[N:7]=[C:6](Cl)[CH:5]=[CH:4][N:3]=1.[CH3:9][O:10][C:11]1[C:16]([O:17][CH3:18])=[C:15]([O:19][CH3:20])[CH:14]=[CH:13][C:12]=1B(O)O.C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1.O>[Cl:1][C:2]1[N:7]=[C:6]([C:12]2[CH:13]=[CH:14][C:15]([O:19][CH3:20])=[C:16]([O:17][CH3:18])[C:11]=2[O:10][CH3:9])[CH:5]=[CH:4][N:3]=1

Komponenten

6

Edukt 3

HCID 10340Sodium CarbonateHCID 775312,4-DichloropyrimidineHCID 27735822,3,4-Trimethoxybenzeneboronic acid

Produkt 1

HCID 223181282-Chloro-4-(2,3,4-trimethoxyphenyl)pyrimidineAusbeute 74,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel2×HCID 1140TolueneLösungsmittel2×

Versuchsvorschrift

In a 250 mL round-bottomed flask, 1.49 grams (10 mmol) of 2,4-dichloropyrimidine was combined with 2,3,4-trimethoxyphenylboronic acid (2.12 g, 10 mmol), sodium carbonate (2.12 g, 2 equivalents), and 1.15 g (0.1 equivalents) of tetrakis-triphenylphosphinepalladium. Toluene (50 mL) and water (5 mL) were added. The reaction was allowed to reflux under nitrogen overnight. The reaction was diluted with toluene and water and the organic layer was separated, washed with brine, dried (Na2SO4), filtered, and concentrated to afford the crude pyrimidine 5. The compound was purified on silica gel using an eluent of 30% acetone/hexane to afford 2.08 g (74%) of the product 5 as a white solid.

Aufarbeitung

  1. temperatureto reflux under nitrogen overnight
  2. customthe organic layer was separated
  3. washwashed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto afford the crude pyrimidine 5
  8. customThe compound was purified on silica gel using an eluent of 30% acetone/hexane

Quellen und Nachweise

ORD-Eintrag
ord-aa6cd608c38a4c91819a1afb07b5b2b6
Quelldatensatz
uspto-grants-2005_09
Patentnummer
US06949544B2

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