Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | HCID 71060343 | HCID 71060343 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 71060547 | HCID 71060547 | 40% |
Reaction Steps
A mixture of tert-butyl 2-(2-chlorooxazol-5-yl)-5-fluoro-1H-indole-1-carboxylate 50 (0.308 g, 0.916 mmol) and commercially available 3-aminophenol 8 (0.10 g, 0.916 mmol) in 2-propanol (20 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, solvent was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate 51 (0.15 g, 40% yield) as solid. MS (ES) m/z 410 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865709B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-0625dda6103c436aa8706e6e4d132dca |
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| Source note | uspto-grants-2014_10 |
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