Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Dibutyl Vinylboronate (stabilized with Phenothiazine) | HCID 236543 | — |
| Reactant | HCID 67155404 | HCID 67155404 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | HCID 68509393 | HCID 68509393 | — |
Reaction Steps
To a mixture of 5′-chloro-N,2′-dimethyl-4′-nitrobiphenyl-4-carboxamide (Step 2, 100 mg, 0.33 mmol), vinylboronic acid dibutyl ester (90 mg, 0.5 mmol) and sodium carbonate (245 mg, 2.31 mmol) in THF/H2O (8/2 mL) is added dichlorobis(triphenylphospine) palladium (II) (12 mg, 5% mmol). The reaction tube is sealed, the mixture is purged with N2 for 3 min and then heated at 90° C. under N2 for overnight. The reaction is cooled to room temperature and poured into saturated aqueous ammonia chloride solution. The crude reaction mixture is extracted with ethyl acetate (3×15 mL). The organic extracts are combined, washed with brine and concentrated. The crude product is purified with silica gel column chromatography (30% ethyl acetate in DCM) to afford N,2′-dimethyl-4′-nitro-5′-vinylbiphenyl-4-carboxamide as a yellow solid. The obtained solid is dissolved in methanol (20 mL). To this solution is added Pd/C (10%). The reaction mixture is degassed and purged with H2 for several times and stirred under atmospheric hydrogen overnight. The mixture is filtered and concentrated to afford 4′-amino-5′-ethyl-N,2′-dimethylbiphenyl-4-carboxamide as a yellow solid. ESMS m/z 269.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440681B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-7dfd4a31849544bf84bd4db5184320ea |
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| Source note | uspto-grants-2013_05 |
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