Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 1,3-Dioxane-4,6-dione, 5-((4-bromophenyl)methylene)-2,2-dimethyl- | HCID 367161 | — |
| Reactant | Sodium Ascorbate | HCID 23667548 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68503211 | HCID 68503211 | 51.3% |
Reaction Steps
A solution of copper (II) acetate monohydrate (10 mg, 0.050 mmol) in water (0.2 ml) was treated with sodium (L)-ascorbate (20 mg, 0.10 mmol), the mixture was stirred until the mixture was turned bright orange (3 min). Subsequently, (R,M)-3-{[4-(2-diphenylphosphanyl-7-methoxy-naphthalen-1-yl)-phthalazin-1-ylamino]-phenyl-methyl}-pentan-3-ol (1st diastereomer, 33.1 mg, 0.050 mmol) and phenylacetylene (0.275 ml, 2.5 mmol) were added, the resulting mixture was stirred for 10 min at 23° C., cooled to 0° C., stirred for 5 min and treated with 5-(4-bromobenzylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione (77.7 mg, 0.25 mmol). The reaction mixture was stirred vigorously at 0° C. for 42 hrs, diluted with dichloromethane (2 ml) and subjected directly to flash chromatography on silica gel (hexane/EtOAc 3:1→1:1) to give 53 mg of the pure title compound as a white solid. (Yield: 39%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790882B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-5ffbc9db60c54654a8d628cb97eeaf31 |
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| Source note | uspto-grants-2010_09 |
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