Sodium hydride → HCID 9927063, Verbindung

HRID 2297401Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2297401
[Cl:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:9])[C:7]=1[CH3:8].[H-].[Na+].Cl[C:13]1[C:22]2[C:17](=[CH:18][C:19]([O:23][CH3:24])=[CH:20][CH:21]=2)[CH:16]=[N:15][N:14]=1>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:9])[C:7]=1[CH2:8][C:13]1[C:22]2[C:17](=[CH:18][C:19]([O:23][CH3:24])=[CH:20][CH:21]=2)[CH:16]=[N:15][N:14]=1

Komponenten

5

Edukt 3

HCID 24758Sodium hydrideHCID 109538273,5-Dichloro-4-methylpyridineHCID 183816081-Chloro-6-methoxyphthalazine

Produkt 1

HCID 9927063HCID 9927063, VerbindungAusbeute 79,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel2×

Versuchsvorschrift

A solution of 3,5-dichloro-4-methyl-pyridine (11.32 g, 70 mmoles) in dry DMF (100 ml) was stirred under N2 at room temperature, then added with 60% NaH in oil (2.8 g, 70 mmoles). After 1 hour at room temperature a solution of 1-chloro-6-methoxy-phthalazine (6.8 g, 35 mmoles), prepared as described in example 4, in DMF (250 ml) was added. The mixture was left at room temperature for 20 hours, then poured into water/ice (pH≅8) and extracted more times with CH2Cl2. The organic phases were washed with water, anhydrified and brought to dryness to give a solid which was triturated in isopropyl ether (100 ml) and filtered. The mother liquors were dried and the residue flash chromatographed with ethyl acetate to give 8.9 g of the title compound (yield: 79.5%). m.p.: 173-175° C.

Aufarbeitung

  1. customprepared
  2. additionwas added
  3. extractionextracted more times with CH2Cl2
  4. washThe organic phases were washed with water
  5. customto give a solid which
  6. customwas triturated in isopropyl ether (100 ml)
  7. filtrationfiltered
  8. customThe mother liquors were dried
  9. customthe residue flash chromatographed with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-665196543dea48f5b4b86a18c74754db
Quelldatensatz
uspto-grants-2002_12
Patentnummer
US06492360B1

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