Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dimethylbarbituric acid | HCID 69860 | — |
| Reactant | HCID 86586687 | HCID 86586687 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86586688 | HCID 86586688 | 85.4% |
Reaction Steps
Tetrakis(triphenylphosphine)palladium(0) (64 mg, 0.055 mmol) was added to a stirred mixture of (1R*,2R*,5S*,6R*)-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-6-cyano-1-phenyl-8-(prop-2-enyl)-8-azabicyclo[3.2.1]octane (Example 55; 500 mg, 1.01 mmol), 1,3-dimethylbarbituric acid (465 mg, 3.0 mmol) in dichloromethane (10 ml) at room temperature. The reaction mixture was stirred at 30-35° C. for 90 minutes and treated with 2M aqueous NaOH (10 ml). The mixture was stirred for 5 minutes, then diluted with water (30 ml) and extracted into dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified by chromatography on silica gel (iso-hexane:ethyl acetate 10-40%) to give the title compound (392 mg, 85%). The hydrochloride salt of the title compound was prepared by treatment with ethereal HCl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727249B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-88a6fdf0ec43426a8beb2139bf5546ef |
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| Source note | uspto-grants-2004_04 |
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