Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | HCID 131724724 | HCID 131724724 | — |
| Solvent | Trimethyl orthoformate | HCID 9005 | — |
| Product | HCID 22591830 | HCID 22591830 | — |
Reaction Steps
A solution of methyl (3-formylphenyl)-5-oxopyrrolidine-3-carboxylate, 2-aminopyridine, and AcOH in trimethylorthoformate was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo and the residue was re-dissolved in methanol. The solution was then cooled to 0° C. AcOH was added followed by NaBH3CN solid in portions. The reaction was allowed to stirred at room temperature for 8 hours. The reaction solution was then concentrated in vacuo. The residue was dissolved in EtOAc and organic solution was washed with saturated NaHCO3 twice. The organic layer was dried over Na2SO4 and concentrated in vacuo. The crude product was purified by silica gel chromatograph (10% meOH/EtOAc) to provide an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06849639B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-e2bc81ed5ea54e5ab82e0fb636dba177 |
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| Source note | uspto-grants-2005_02 |
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