Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzophenone imine | HCID 136809 | — |
| Reactant | (1,1'-Binaphthalen)-2-yldi-tert-butylphosphine | HCID 2734941 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | cis-4-(5-Bromopyridin-2-yl)-1-(2-methyltetrahydrofuran-3-yl)piperidine-4-carbonitrile | HCID 86692463 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86692464 | HCID 86692464 | — |
Reaction Steps
Benzophenonimine (570 mg) was added to a suspension of cis-4-(5-bromopyridin-2-yl)-1-(2-methyltetrahydrofuran-3-yl)piperidine-4-carbonitrile (1.05 g), palladium (II) acetate (17 mg), racemic-2-(di-tert-butylphosphino)-1,1′-binaphthyl (47 mg) and sodium tert-butoxide (432 mg) in toluene (7.5 ml) and stirred at 120° C. for 7 hours. It was left stand and a mixture of concentrated hydrochloric acid (2 ml) and water (6 ml) was added at 60-80° C. and stirred at room temperature for 24 hours. The reaction solution was filtered through Celite and washed with water and ethyl acetate. The filtrate was washed with ethyl acetate, 1N aqueous solution of sodium hydroxide was added to the aqueous layer and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting solid was washed with ethyl acetate and n-hexane to give the titled compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150555B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-b5d96157dc3344b688f2b78df05a2d50 |
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| Source note | uspto-grants-2015_10 |
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