Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 86703281 | HCID 86703281 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86703280 | HCID 86703280 | 68.3% |
Reaction Steps
To a solution of methyl 6-[(2-furan-3-yl-6-methoxy-1H-indol-3-yl)hydroxymethyl]pyridine-2-carboxylate (590 mg) and a boran-2-picoline complex (175 mg) in methanol (3 mL) was added acetic acid (3 mL), and this mixture was stirred at room temperature for 8 hours. The reaction mixture was diluted with ethyl acetate, washed with 5% aqueous sodium hydrogen carbonate solution and saturated brine successively, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (386 mg). 1H-NMR (CDCl3) δ ppm: 3.85 (3H, s), 4.05 (3H, s), 4.48 (2H, s), 6.62-6.67 (1H, m), 6.76 (1H, dd, J=2.3, 8.5 Hz), 6.87-6.91 (1H, m), 7.17-7.23 (1H, m), 7.34 (1H, d, J=8.5 Hz), 7.47-7.52 (1H, m), 7.62 (1H, t, J=7.8 Hz), 7.78-7.84 (1H, m), 7.90-8.06 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815903B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-fc992c822a9f4fb791ce5dfabae65d27 |
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| Source note | uspto-grants-2014_08 |
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