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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 3-benzyl-6-bromoquinazolin-4(3H)-one | HCID 1187507 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Benzyl-4-oxo-6-(2-trimethylsilylethynyl)-3,4-dihydroquinazoline | HCID 23158298 | 107.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902369B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-53dd503f7b9c44f78feb09172bb84bf7 |
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| Source note | uspto-grants-2011_03 |
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