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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219721Generated: October 29, 2026

Potassium Carbonate → 2-tert-Butyl-4-cyclobutyl-6-{4-[3-(pyrimidin-4-yloxy)-propyl]-piperazin-1-yl}-pyrimidine

https://huagongshe.com/reaction/219721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-tert-Butyl-4-[4-(3-chloro-propyl)-piperazin-1-yl]-6-cyclobutyl-pyrimidineHCID 66673104—
ReactantHCID 178516514HCID 178516514—
SolventDimethylformamideHCID 6228—
Product2-tert-Butyl-4-cyclobutyl-6-{4-[3-(pyrimidin-4-yloxy)-propyl]-piperazin-1-yl}-pyrimidineHCID 11668710—

Reaction Conditions

Temperature90 °C

Reaction Steps

0.2 g of 4-hydroxy-pyrimidine (2.08 mmol) were dissolved in 15 ml of dimethylformamide. After addition of 0.58 g of potassium carbonate (4.16 mmol) and 0.73 g of 2-tert-butyl-4-[4-(3-chloro-propyl)-piperazin-1-yl]-6-cyclobutyl-pyrimidine (2.08 mmol), the mixture was stirred at 90° C. for 3 h. The dimethylformamide was removed under reduced pressure and the resulting residue was partitioned between 40 ml of ethyl acetate and 20 ml of water. The aqueous phase was re-extracted with ethyl acetate, the organic layers were combined, dried over magnesium sulfate, filtered, and concentrated to dryness. The crude product was purified by chromatography on silica gel with ethyl acetate-methanol (2-10%). Fractions containing the product were combined. The solvent was evaporated. The product crystallized upon standing (yield: 0.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202868B2
Source datasetuspto-grants-2012_06
ORD IDord-70bde65aa1254fc1ac25f1928c782f03
Source noteuspto-grants-2012_06