Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline | HCID 2734620 | — |
| Reactant | HCID 178502465 | HCID 178502465 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178502467 | HCID 178502467 | 78.5% |
Reaction Steps
To a solution of ((S)-1-{(2S,4S)-2-[4-(4-bromo-phenyl)-1H-imidazol-2-yl]-4-hydroxy-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester (1.8 g, 3.87 mmol) in dioxane (30 mL) and water (10 mL), 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylamine (848 mg, 3.87 mmol), sodium carbonate (820 mg, 7.74 mmol) and Pd(dppf)Cl2 (316 mg, 0.39 mmol) were added and the reaction mixture was heated at reflux for 3 h, cooled to RT, filtered and concentrated, extracted with EtOAc (50 mL), and washed with water (50 mL). The organic layer was dried over sodium sulfate, filtered, concentrated and purified by silica gel column chromatography (eluted with 1% to 3% methanol in DCM) to give the title intermediate (1.45 g, 65% yield). 1H NMR (CH3OD, 400) δ (ppm) 7.70 (m, 2H), 7.67 (m, 2H), 7.45 (m, 2H), 7.29 (s, 1H), 6.80 (d, J=6.8 Hz, 1H), 5.82 (d, J=9.2 Hz, 1H), 5.29 (d, J=8.8 Hz, 1H), 4.59 (s, 1H), 4.34 (d, J=8.8 Hz, 1H), 4.16 (d, J=8.0 Hz, 1H), 3.95-4.04 (m, 1H), 3.79-3.83 (m, 1H), 3.76 (s, 3H), 2.55-2.69 (m, 1H), 2.32 (m, 1H), 1.60-2.03 (m, 1H), 1.00 (m, 3H), 0.3-0.85 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212168B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-6e9bb3d0516845289bae55c1562ca26a |
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| Source note | uspto-grants-2015_12 |
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