Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-Methylindole-3-carboxylic acid | HCID 854040 | — |
| Reactant | HCID 58779051 | HCID 58779051 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58778970 | HCID 58778970 | 71% |
Reaction Steps
1-Methyl-1H-indole-3-carboxylic acid (700 mg, 4.0 mmol) was dissolved in methylene chloride (8 ml). Oxalyl chloride (0.53 ml, 6.1 mmol) was added dropwise to the solution under stirring at 0° C. After completion of the dropwise addition, the reaction mixture was stirred at room temperature for 1 hour and distilled under reduced pressure to remove the solvent. The residue was dissolved in methylene chloride (6 ml). The resulting solution was added to a solution of triethylamine (0.84 ml, 6.0 mmol) and ethyl 4-amino-2-fluoro-5-methoxyphenylacetate (909 mg, 4.0 mmol) in methylene chloride (3 ml) under stirring at 0° C. The reaction mixture was heated at reflux for 18 hours. After cooling to room temperature, the reaction mixture was poured into ice water, followed by extraction with chloroform. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (middle pressure Yamazen, linear gradient of n-hexane/ethyl acetate form 9:1 to 7:3, 12 ml/min, φ 50 mm×300 mm, charged by dry silica gel method). The purified ester was added with THF (45 ml) and 0.25M NaOH (18 ml, 4.5 mmol), followed by stirring at room temperature for 4 hours. The reaction mixture was poured into water and 1M HCl was added to the resulting mixture to make it acidic. The crystals thus precipitated were collected by filtration under reduced pressure, washed with water and dried under reduced pressure to give 2-fluoro-5-methoxy-4-((1-methyl-1H-3-indolylcarbonyl)amino)phenylacetic acid (1.01 g, 71%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-ec829fd900f74d9e99405aa978c07066 |
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| Source note | uspto-grants-2007_01 |
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