Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | HCID 44123674 | HCID 44123674 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 44194571 | HCID 44194571 | 10% |
Reaction Steps
A mixture of (R)-1-((S)-1-(4-bromophenyl)ethyl)-4-(2-hydroxyethyl)-4-phenyl piperidin-2-one (30 mg, 0.072 mmol), 4-fluorophenylboronic acid (15 mg, 0.11 mmol), Pd(Ph3P)2Cl2 (5 mg), and aqueous Cs2CO3 (0.1 mL, 2M) in 1,4-dioxane (2 mL) was stirred and heated at reflux for 2 h. The organic phase was separated, and concentrated to give the crude product, which was purified by preparative TLC to give (R)-1-((S)-1-(4′-fluorobiphenyl-4-yl)ethyl)-4-(2-hydroxyethyl)-4-phenylpiperidin-2-one (3.0 mg, 10%). LC-MS Method 2, tR=2.103 min, m/z=440.1. 1H NMR (CDCl3): δ 1.46 (d, 3H), 1.83 (m, 1H), 2.01 (m, 3H), 2.32 (m, 1H), 2.59 (dd, 1H), 2.96 (m, 1H), 3.11 (dd, 1H), 3.34 (m, 1H), 3.49 (m, 1H), 6.02 (q, 1H), 6.89 (m, 2H), 7.06 (m, 2H), 7.22 (m, 2H), 7.31 (m, 4H), 7.40 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680281B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-448d68c6c3f743c6a934feafc0bf5feb |
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| Source note | uspto-grants-2014_03 |
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