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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244811Generated: November 1, 2026

Potassium Carbonate → 2-(6-quinazolinoxy)-N-(4-methylpent-2-yn-4-yl) butyramide

https://huagongshe.com/reaction/1244811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantQuinazolin-6-olHCID 589643—
Reactant2-bromo-N-(4-methylpent-2-yn-4-yl)butyramideHCID 21078406—
ReactantEthyl acetate hexaneHCID 21226206—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(6-quinazolinoxy)-N-(4-methylpent-2-yn-4-yl) butyramideHCID 6925497093.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

6-Hydroxyquinazoline (0.060 g, prepared as described in J. Chem. Soc. (1952), 4985) and 2-bromo-N-(4-methylpent-2-yn-4-yl) butyramide (0.101 g) were dissolved in dry N,N-dimethylformamide (2 ml) containing anhydrous potassium carbonate (0.088 g). The mixture was stirred and heated to 80° C. for 5 hours then allowed to cool to ambient temperature and stored for 18 hours. The brown suspension was diluted with water, extracted into ethyl acetate and the organic phase separated, washed with water, dried over magnesium sulphate and evaporated under reduced pressure to give a pale brown oil. The oil was fractionated by chromatography (silica; ethyl acetate/hexane, 4:1 by volume) to give the title product (0.12 g) as a pale brown gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122672B2
Source datasetuspto-grants-2006_10
ORD IDord-0577450bb10c46ae8d4107c21ed17d1c
Source noteuspto-grants-2006_10