Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178469456 | HCID 178469456 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178524688 | HCID 178524688 | 99.7% |
Reaction Steps
Ethyl 3-bromo-7-hydroxypyrazolo[1,5-a]pyrimidine-6-carboxylate (Journal of Medicinal Chemistry, vol. 25, p. 235, 1982) (11.0 g, 38.5 mmol) was dissolved in ethanol (134 mL), 2 mol/L aqueous sodium hydroxide solution (134 mL, 269 mmol) was added, and the mixture was stirred at 60° C. for 1 hr. The reaction mixture was cooled to room temperature, and ethanol was evaporated under reduced pressure. 2 mol/L Hydrochloric acid (140 mL) was added under ice-cooling, and the mixture was stirred at room temperature for 30 min. The precipitate was collected by filtration, and washed with water (100 mL) and 2-propanol (50 mL) to give the title compound (9.9 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729264B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-84dd34bdb76e4046937cdae061b624aa |
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| Source note | uspto-grants-2014_05 |
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