Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 5195952 | HCID 5195952 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57901672 | HCID 57901672 | 97.2% |
Reaction Steps
A mixture of ethyl 7-{[2-(methylsulfonyl)phenylsulfonyl]amino}-1H-indole-2-carboxylate (1.84 g), 8N aqueous sodium hydroxide solution (2.50 mL), tetrahydrofuran (5 mL) and methanol (5 mL) was stirred at 60° C. for 2 hr. The reaction mixture was concentrated, and water was added to the residue. The mixture was acidified with 10% aqueous citric acid solution, and the resulting crystals were filtrated, washed with water, and dried to give the title compound (1.67 g, yield 97%) as yellow crystals. melting point>304° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957070B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-5ed87a3495b0407db390b1d64901f284 |
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| Source note | uspto-grants-2015_02 |
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