Diisopropylethylamine → (2-Cyclopropyl-6-chloro-5-methyl-pyrimidin-4-yl]-[1,8]naphthyridine

HRID 1169809

Reaktionsgleichung

Reaktionsgleichung von HRID 1169809
C(N(C(C)C)CC)(C)C.[CH:10]1([C:13]2[N:18]=[C:17]([Cl:19])[C:16]([CH3:20])=[C:15](Cl)[N:14]=2)[CH2:12][CH2:11]1.N1CCC([C:28]2[CH:37]=[CH:36][C:35]3[C:30](=[N:31][CH:32]=[CH:33][CH:34]=3)[N:29]=2)CC1.N1C2C(=CC=CN=2)C=CC=1.C(=O)(O)[O-].[Na+]>O.C(OCC)(=O)C.CC(N(C)C)=O>[CH:10]1([C:13]2[N:14]=[C:15]([C:28]3[CH:37]=[CH:36][C:35]4[C:30](=[N:31][CH:32]=[CH:33][CH:34]=4)[N:29]=3)[C:16]([CH3:20])=[C:17]([Cl:19])[N:18]=2)[CH2:11][CH2:12]1

Komponenten

9

Edukt 5

HCID 81531DiisopropylethylamineHCID 1360691,8-NaphthyridineHCID 516892Sodium BicarbonateHCID 545957314,6-Dichloro-2-cyclopropyl-5-methylpyrimidineHCID 666409192-(Piperidin-4-YL)-1,8-naphthyridine

Produkt 1

HCID 86761204(2-Cyclopropyl-6-chloro-5-methyl-pyrimidin-4-yl]-[1,8]naphthyridineAusbeute 66,1 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 8857Ethyl AcetateLösungsmittelHCID 31374DimethylacetamideLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

20 ml of dimethylacetamide and 3.36 ml (19.2 mmoles) of diisopropylethylamine are added into a single-necked flask containing 1.5 g (7.39 mmoles) of 2-cyclopropyl-4,6-dichloro-5-methyl-pyrimidine and 1.58 g (7.39 mmoles) of 2-piperidin-4-yl-[1,8]naphthyridine. This mixture is heated at 100° C. overnight. The next day 0.2 equivalent of naphthyridine is added and the reaction mixture is heated for another 6 hours, followed by returning to ambient temperature before concentration to dryness. The residue obtained is taken up in a mixture of water, ethyl acetate and a saturated solution of sodium bicarbonate. The organic phase is separated and the aqueous phase reextracted with ethyl acetate. The collected organic phases are dried over magnesium sulphate then the solvent is evaporated off under reduced pressure (2 kPa). The residue is chromatographed on silica gel eluting with a gradient of heptane-ethyl acetate (50-50) to 100% ethyl acetate, 1.45 g of expected product is obtained.

Aufarbeitung

  1. temperaturethe reaction mixture is heated for another 6 hours
  2. concentrationby returning to ambient temperature before concentration to dryness
  3. customThe residue obtained
  4. customThe organic phase is separated
  5. dry with materialThe collected organic phases are dried over magnesium sulphate
  6. customthe solvent is evaporated off under reduced pressure (2 kPa)
  7. customThe residue is chromatographed on silica gel eluting with a gradient of heptane-ethyl acetate (50-50) to 100% ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-70a61eec63e4482caa4dbe0d8319cd2d
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07825119B2

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