HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566181Generated: November 1, 2026
Trimethylsilylacetylene → HCID 70220561, compound
https://huagongshe.com/reaction/566181
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | HCID 21265540 | HCID 21265540 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 70220561 | HCID 70220561 | 33.4% |
Reaction Steps
3-(7-Bromo-5-fluoro-2-methyl-2,3-dihydrobenzo[b]furan-4-yl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione (1.15 g), trimethylsilylacetylene (0.53 g), a palladium chloride-ditriphenylphosphine complex (95 mg) and copper(I) iodide (27 mg) was suspended in triethylamine (11 ml) and DMF (3 ml), and the mixture was stirred at 50° C. for 12 hours. After the reaction, triethylamine was distilled off under reduced pressure. Ethyl acetate was added thereto, and the insolubles were filtered. Then, ethyl acetate was distilled off, and the resulting residue was purified by chromatography on silica gel (ethyl acetate:n-hexane=1:3 v/v) to obtain the objective 3-{5-fluoro-2-methyl-7-[2-(trimethylsilyl)-1-ethynyl]-2,3-dihydrobenzo[b]furan-4-yl}-1-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione (0.40 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174839B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-eceaa87879384386aed24bfb954e782d |
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| Source note | uspto-grants-2001_01 |
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