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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601657Generated: October 29, 2026

Triethylamine → 3-Benzyl-4-oxo-6-(2-trimethylsilylethynyl)-3,4-dihydroquinazoline

https://huagongshe.com/reaction/601657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant3-benzyl-6-bromoquinazolin-4(3H)-oneHCID 1187507—
CatalystCopper iodideHCID 83717—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDimethylformamideHCID 6228—
Product3-Benzyl-4-oxo-6-(2-trimethylsilylethynyl)-3,4-dihydroquinazolineHCID 23158298107.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

Under nitrogen atmosphere, 947 mg of trimethylsilylacetylene, 54.7 mg of copper iodide (I), 54.2 mg bis(triphenylphosphine) palladium dichloride (II) and 3 ml of triethylamine were added sequentially to 1.5 ml solution of dimethylformamide with 501 mg of 3-benzyl-6-bromo4-oxo-3,4-dihydroquinazoline, and the mixture was stirred at 100° C. for 14 hours. After distilling out the solvents under reduced pressure, water was added to the reaction solution, and extracted with ether. Ether layer was washed with saturated saline solution, and dried with anhydrous sodium sulfate. The solvents were distilled outunder reduced pressure, and the residues were separated and purified by silicagel column chromatography (ethyl acetate/hexane=3/7) to obtain 570 mg of the above compound as a colorless oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-53dd503f7b9c44f78feb09172bb84bf7
Source noteuspto-grants-2011_03