Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Fluoroindole | HCID 67861 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22997492 | HCID 22997492 | 73% |
Reaction Steps
A stirred solution of 5-fluoroindole (4 g, 30 mmol) in methanol is treated with 3-pyridine carboxaldehyde (2.79 ml, 30 mmol), cooled to 0° C., treated with 50% NaOH (3.25 ml), stirred at 0° C. for 1 hr, warmed to room temperature, stirred for 3 hr, treated with water and extracted with ethyl acetate. The extracts are combined, dried over Na2SO4 and concentrated in vacuo. The residue is treated with ethyl acetate and filtered. The filtrate is further concentrated and filtered. The filtercakes are combined and dried to afford the title compound as a pale orange solid 5.2 g (73%) mp 131-133° C., identified by NMR and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613781B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-4d2c2c917c5e46b1a9f120febd5d96e7 |
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| Source note | uspto-grants-2003_09 |
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