Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Bromo-5-fluoropyridine-4-carboxaldehyde | HCID 53429192 | — |
| Reactant | 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2(3H)-benzoxazolone | HCID 59535069 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86663361 | HCID 86663361 | 35% |
Reaction Steps
A mixture of 3-Methyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3H-benzooxazol-2-one (138 mg, 0.5 mmol), 3-Bromo-5-fluoro-pyridine-4-carbaldehyde (102 mg, 0.5 mmol), Na2CO3 (2 M in water, 0.75 mL, 1.5 mmol) and PdCl2(PPh3)2 (17 mg, 0.03 mmol) in DMF (3 mL) was heated at 100° C. for 4 hrs. After concentration, the residue was diluted with DCM and saturated NH4Cl solution. After filtration and concentration, the residue was purified by flash column (MeOH—CH2Cl2, v/v, 0-1.5%) and afforded the title compound (47 mg, 35%). 1H NMR (400.3 MHz, CDCl3): δ 3.45 (s, 3H), 6.96 (d, J=1.7 Hz, 1H), 7.08 (dd, J=8, 1.7 Hz, 1H), 7.32 (d, J=8 Hz, 1H) 8.59 (s, 1H), 8.68 (d, J=1.3 Hz, 1H), 10.07 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455522B2 |
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| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-3a01f5c5f44e4df09531d5fbcecea7b5 |
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| Source note | uspto-grants-2013_06 |
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