Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine | HCID 353442 | — |
| Reactant | HCID 23498515 | HCID 23498515 | — |
| Product | HCID 131724526 | HCID 131724526 | 83% |
Reaction Steps
To a solution of tert-butyl 8-[(1E)-3-ethoxy-3-oxo-1-propenyl]-3,4-dihydro-1(2H) -quinolinecarboxylate (2.55 g, 7.7 mmol) in 50 mL of methylene chloride at 0° C. was added N-(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine (4.6 g, 19.3 mmol) and trifluoroacetic acid (0.24 mL, 3.1 mmol). The cooling bath was removed and the solution was allowed to stir with warming to ambient temperature for 24 h. The methylene chloride was removed under reduced pressure. The residue was dissolved in ethyl acetate, washed with saturated aqueous sodium bicarbonate and brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography (elution with 5:1 hexane/ethyl acetate) to afford 3.0 g (83%) of the title compound as an oil. LRMS (ES)+: 465.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777406B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-67b2d350e2f9483b9d9c6780a49acaae |
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| Source note | uspto-grants-2004_08 |
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