Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3-Dimethyl-4-nitropyridine-N-oxide | HCID 148223 | — |
| Reactant | 4-Bromo-3-fluorophenol | HCID 2779153 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59287327 | HCID 59287327 | 175.5% |
Reaction Steps
To a room temperature solution of 4-bromo-3-fluorophenol (15 g, 78.53 mmol) in DMF (50 ml) was added sodium hydride (3.32 g, 85.67 mmol, 60% in mineral oil) portionwise. After stirring for 10 minutes 2,3-dimethyl-4-nitro-pyridine 1-oxide (1.05 g, 6.28 mmol) was added The reaction mixture was heated at 180° C. for 60 minutes under microwave irradiation. After cooling to room temperature the mixture was filtered through a diatomaceous earth pad and the filtrate was then diluted with EtOAc and washed with water. The solution was then extracted with additional EtOAc (2×150 ml). The organic layer was dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; DCM to DCM/MeOH up to 5% as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate 21 (3.44 g, 19%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067891B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-01ed3c7910e94c038feadd0092acfb89 |
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| Source note | uspto-grants-2015_06 |
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