Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Bromo-1-methyl-1H-imidazole | HCID 1515258 | — |
| Reactant | HCID 22285041 | HCID 22285041 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | HCID 20767729 | HCID 20767729 | 72.4% |
Reaction Steps
To a mixture of methyl-3-(4,4,5,5,-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-naphthoate (Preparation 13) (15.37 g, 49.3 mmol) and 5-bromo-1-methyl-1H-imidazole (9.06 g, 49.3 mmol) in toluene/EtOH (350 mL/36 mL) were added Pd(PPh3)4 (11.37 g, 9.84 mmol), Na2CO3 (20.9 g, 197.2 mmol) and water (106 mL). The mixture was degassed, purged with N2, and heated to reflux for 20 hours. It was then cooled to RT, neutralized with HCl (1.0 N, 100 mL), and concentrated in vacuo. The residue was partitioned between water (300 mL) and EtOAc (1 L). The organic layer was washed with water (2 L) and brine, dried over MgSO4, filtered and evaporated in vacuo. The resulting crude material was submitted to flash chromatography (1.5% MeOH/CHCl3), furnishing the title compound as a light-yellow solid (9.5 g, 72%). 1H NMR (CDCl3): 8.53 (s, 1H), 7.99 (d, J=8.1, 1H), 7.80 (d, J=8.1, 1H), 7.77 (s, 1H), 7.56 (m, 1H), 7.54 (m, 1H), 7.54 (s, 1H), 6.94 (s, 1H), 3.73 (s, 3H), 3.29 (s, 3H). (ESI) m/z (M+H)+=267.11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06869956B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-9a79fa7065e548a28a4cf951f817df57 |
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| Source note | uspto-grants-2005_03 |
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