Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67070018 | HCID 67070018 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67069927 | HCID 67069927 | 66.2% |
Reaction Steps
step 5—A mixture of 86 (0.050 g, 0.11 mmol), 48% HBr (0.050 mL) and AcOH (2 mL) in a sealed tube was heated overnight at 70° C. The reaction mixture was cooled to RT, carefully poured into a cold saturated aqueous NaHCO3 and then extracted with EtOAc. The organic layer was washed with brine, dried (MgSO4) and concentrated. The crude residue was purified by SiO2 chromatography and eluted with 10% MeOH/DCM to afford 32 mg (66%) of N-(4-{2-[2-amino-5-tert-butyl-3-(2-oxo-1,2-dihydro-pyridin-3-yl)-phenyl]-ethyl}-phenyl)-methanesulfonamide (88) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273773B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-b3afb77292c442f98a58dc95d92e9cc1 |
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| Source note | uspto-grants-2012_09 |
|---|