Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 66680081 | HCID 66680081 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66679802 | HCID 66679802 | 53% |
Reaction Steps
20 mL of THF and 2.6 mL of 1N aqueous sodium hydroxide were added to 0.32 g (0.87 mmol) of methyl 5-chloro-2-({[3-(pyridin-4-yl)phenyl]carbonyl}amino)benzoate at room temperature, and the mixture was stirred at 50° C. for 1 hour. After cooling, the solvent was distilled off under reduced pressure, and water was added to the residue, followed by filtration and drying, thereby giving 174 mg of the target sodium 5-chloro-2-({[3-(pyridin-4-yl)phenyl]carbonyl}amino)benzoate (yield: 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785473B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-e2674664f2b940a5b617f2462284da82 |
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| Source note | uspto-grants-2014_07 |
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