Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | 6-(4-Chloro-benzoyl)4-(3-iodo-phenyl)-1-methyl-1H-quinolin-2-one | HCID 15489630 | — |
| Catalyst | 1,4-Bis(diphenylphosphino)butane | HCID 82124 | — |
| Catalyst | Bis(benzonitrile)palladium chloride | HCID 498840 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18379026 | HCID 18379026 | 85.8% |
Reaction Steps
To a solution of 1,4-bis(diphenylphosphine)butane (120 mg, 0.28 mMol) in toluene (15 mL) was added dichlorobis(benzonitrile)palladium(II) (108 mg, 0.28 mMol) under an atmosphere of dry N2. The reaction mixture was stirred at ambient temperature for 45 minutes after which time the solution was diluted with toluene (85 mL). To this solution was added 6-(4-chloro-benzoyl)-4-(3-iodo-phenyl)-1-methyl-1H-quinolin-2-one (14.0 g, 28.0 mMol) and tributyl(vinyl)tin (9.1 mL, 32.9 mMol). The reaction was heated to reflux and stirred at this temperature for 1 hour. The reaction mixture was concentrated under vacuum and chromatographed on flash silica gel eluting DCM until the tin impurities had eluted. The product was eluted off with DCM/MeOH (99:1) to give 9.61 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495564B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-4ecc4dd1316c419485b48e657f760aaf |
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| Source note | uspto-grants-2002_12 |
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