Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21475300 | HCID 21475300 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21475297 | HCID 21475297 | 102.1% |
Reaction Steps
To a solution of 7-(2-methoxycarbonylphenyl)amino-5-methylpyrazolo[1,5-a]pyrimidine (1.0 g) prepared in Example 3 in ethanol (20 ml) is added a 5% sodium hydroxide solution (30 ml), and the mixture is heated with stirring at 100° C. for one hour. After cooling, the mixture is evaporated to remove ethanol, and the residue is neutralized with a 10% hydrochloric acid, and further the pH value of the mixture is adjusted to pH 4 with a saturated aqueous citric acid solution. The precipitated crystal is collected by filtration, and washed with water, ethanol and ethyl ether, and dried to give 7-(2-carboxyphenyl)amino-5-methylpyrazolo[1,5-a]pyrimidine (970 mg) as colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05688949 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-13c5ff9f51eb42469b2f12cdd52456f6 |
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| Source note | uspto-grants-1997_11 |
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