Dimethylacetamide → 4-Bromo-5-ethyl-6-[4-(aminomethyl-2-pyridinyl)-1-piperidinyl]-pyrimidine

HRID 2358221Notizen

Reaktionsgleichung

C([N:4]([CH:7]([CH3:9])[CH3:8])[CH2:5][CH3:6])(C)C.Br[C:11]1[C:16]([CH2:17][CH3:18])=[C:15]([Br:19])[N:14]=[CH:13][N:12]=1.CC1[CH2:26][CH2:25][N:24](NC2C=CC=CN=2)[CH2:23][CH2:22]1.[C:34](=O)(O)[O-].[Na+].[CH3:39][N:40](C)C(=O)C>C(OCC)(=O)C.O>[Br:19][C:15]1[C:16]([CH2:17][CH3:18])=[C:11]([N:24]2[CH2:25][CH2:26][CH:9]([C:7]3[C:8]([CH2:39][NH2:40])=[CH:34][CH:6]=[CH:5][N:4]=3)[CH2:22][CH2:23]2)[N:12]=[CH:13][N:14]=1

Komponenten

Reaktionsbedingungen

Temperatur: 110 °C

Versuchsvorschrift

1.8 ml of diisopropylethylamine is added to a mixture of 657 mg (2.47 mmoles) of 4,6-dibromo-5-ethyl-pyrimidine and 450 mg (2.35 mmoles) of 2-(4-methylpiperidinyl)aminopyridine in 55 ml of N,N-dimethylacetamide. This mixture is heated at 110° C. for 4 hours. Then the solvent is eliminated under reduced pressure (0.2 kPa) and the residue is taken up in a mixture of ethyl acetate, water and a saturated solution of sodium bicarbonate. The organic phase is decanted, dried over magnesium sulphate then condensed under reduced pressure (2 kPa). The brown oil obtained is chromatographed on alumina eluting with the following gradient: heptane-ethyl acetate 80-20 to 70-30. 747 mg (Yield=84%) of expected product is obtained in the form of a beige solid.

Aufarbeitung

customThe organic phase is decanted
dry with materialdried over magnesium sulphate
customcondensed under reduced pressure (2 kPa)
customThe brown oil obtained
customis chromatographed on alumina eluting with the following gradient

Quellen und Nachweise

ORD-Eintrag: ord-8d551b1ce3854d61b7b68768a9c3a53a
Quelldatensatz: uspto-grants-2010_07
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07763621B2

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