HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 67609817, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 67608713 | HCID 67608713 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 67609817 | HCID 67609817 | 29% |
Reaction Conditions
| Temperature | 105 °C |
|---|
Reaction Steps
Compound 67 (581.6 mg, 1.431 mmol) obtained in Example 63 was dissolved in tert-butanol (48 mL), and pyrimidium p-toluenesulfonate (3.6 g; 14 mmol) was added thereto, followed by stirring at 105° C. for 4 hours. The reaction mixture was cooled to 0° C., a saturated aqueous ammonium chloride solution was added, followed by extraction with ethyl acetate (50 mL×3). The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated to yield a residue. The residue was purified by silica gel column chromatography, followed by purification by high-speed liquid chromatography (60 to 100% acetonitrile/water) to obtain the title compound (150 mg, 29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952003B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-9239e60779b14a98a97fb602a85691fb |
| Source note | uspto-grants-2015_02 |