Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium acetate | HCID 3474584 | — |
| Reactant | 1-(tert-Butyldimethylsilyloxy)-1-methoxyethene | HCID 4564491 | — |
| Reactant | HCID 86642382 | HCID 86642382 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67457614 | HCID 67457614 | — |
Reaction Steps
A mixture of trifluoromethanesulfonic acid 8-chloro-2-isopropyl-4-methyl-3-(4-pyrazol-1-ylbenzyl)quinolin-5-yl ester (0.075 g), tert-butyl-(1-methoxyvinyloxy)dimethylsilane (0.063 mL), lithium acetate (0.029 g) and tetrahydrofuran (2.0 mL) was purged with argon for 30 minutes, and then treated with tetrakis(triphenylphosphine)palladium (0) (0.017 g). The mixture was stirred at 70° C. for four days, cooled to room temperature and filtered through Celite. The filtrate was concentrated under reduced pressure and the residue purified by column chromatography on silica gel, eluting with a mixture of cyclohexane and ethyl acetate (10:0 to 2:8 by volume) to give title compound as pale yellow oil (0.042 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394830B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-e48d6304c2ac41428de0dea8db2515eb |
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| Source note | uspto-grants-2013_03 |
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