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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358221Generated: October 26, 2026

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

https://huagongshe.com/reaction/2358221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-Methylpiperidinyl)aminopyridineHCID 20453758—
Reactant4,6-Dibromo-5-ethyl-pyrimidineHCID 57832894—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-Bromo-5-ethyl-6-[4-(aminomethyl-2-pyridinyl)-1-piperidinyl]-pyrimidineHCID 8660360684%

Reaction Conditions

Temperature110 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763621B2
Source datasetuspto-grants-2010_07
ORD IDord-8d551b1ce3854d61b7b68768a9c3a53a
Source noteuspto-grants-2010_07