Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 23020386 | HCID 23020386 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Product | HCID 57526918 | HCID 57526918 | — |
Reaction Steps
In 20 ml of ethanol were suspended 1 g of 4-(2-chloropyridin-4-yl)-3-(4-fluorophenyl)-1-(2-cyanobenzyl)-4-imidazolin-2-one [Compound of Reference example 1(6)], 55 mg of palladium acetate, 137 mg of 1,1′-bis(diphenylphosphino)ferrocene and 608 mg of sodium acetate, the mixture was stirred under carbon monoxide atmosphere at 80° C. for 12 hours. The reaction mixture was concentrated under reduced pressure, the residue was suspended in ethyl acetate, treated with activated charcoal and then filtered. After concentration under reduced pressure, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:2) to give 887 mg of the title compound as colorless crystal. Melting point: 164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846933B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-8fd9dbc2245243368f885d26c9e6c553 |
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| Source note | uspto-grants-2010_12 |
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