Sodium Carbonate → N-Methyl-5-[6-morpholin-4-yl-9-(tetrahydrofuran-3-ylmethyl)-9H-purin-2-yl]pyrimidin-2-amine

HRID 1876513Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1876513
O1CCOCC1.C(=O)([O-])[O-].[Na+].[Na+].[CH3:13][NH:14][C:15]1[N:20]=[CH:19][C:18](B2OC(C)(C)C(C)(C)O2)=[CH:17][N:16]=1.Cl[C:31]1[N:39]=[C:38]2[C:34]([N:35]=[CH:36][N:37]2[CH2:40][CH:41]2[CH2:45][CH2:44][O:43][CH2:42]2)=[C:33]([N:46]2[CH2:51][CH2:50][O:49][CH2:48][CH2:47]2)[N:32]=1>O>[CH3:13][NH:14][C:15]1[N:16]=[CH:17][C:18]([C:31]2[N:39]=[C:38]3[C:34]([N:35]=[CH:36][N:37]3[CH2:40][CH:41]3[CH2:45][CH2:44][O:43][CH2:42]3)=[C:33]([N:46]3[CH2:47][CH2:48][O:49][CH2:50][CH2:51]3)[N:32]=2)=[CH:19][N:20]=1

Komponenten

6

Edukt 4

HCID 10340Sodium CarbonateHCID 312751,4-DioxaneHCID 467396412-Methylaminopyrimidine-5-boronic acid, pinacol esterHCID 593335062-Chloro-6-morpholin-4-yl-9-(tetrahydrofuran-3-ylmethyl)-9H-purine

Produkt 1

HCID 59333550N-Methyl-5-[6-morpholin-4-yl-9-(tetrahydrofuran-3-ylmethyl)-9H-purin-2-yl]pyrimidin-2-amineAusbeute 41 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

1,4-Dioxane (40 ml), water (20 ml), and sodium carbonate (2 g, 19 mmol) were added to N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine (1.45 g, 6.18 mmol) and 2-chloro-6-morpholin-4-yl-9-(tetrahydrofuran-3-ylmethyl)-9H-purine (2.0 g, 6.18 mmol) and the atmosphere in the reaction vessel was substituted with nitrogen. Tetrakis triphenylphosphine palladium (0.36 g, 0.31 mmol) was added, then the atmosphere in the reaction vessel was substituted with nitrogen again, and the resulting mixture was heated to reflux for 3 hours. The reaction mixture was partitioned with ethyl acetate and water, the organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. Methylene chloride-ether was added to the residue and the insoluble matter was collected by filtration and dried to give the title compound (1.0 g, 41%) as a white solid.

Aufarbeitung

  1. temperaturethe resulting mixture was heated
  2. temperatureto reflux for 3 hours
  3. customThe reaction mixture was partitioned with ethyl acetate and water
  4. dry with materialthe organic layer was dried over magnesium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. additionMethylene chloride-ether was added to the residue
  7. filtrationthe insoluble matter was collected by filtration
  8. customdried

Quellen und Nachweise

ORD-Eintrag
ord-84d40d39c55349ea87b9b9d71b504a86
Quelldatensatz
uspto-grants-2012_11
Patentnummer
US08309546B2

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