Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 5-fluoro-1,3-dihydro-2H-indol-2-one | HCID 3731012 | — |
| Reactant | HCID 67314944 | HCID 67314944 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67314578 | HCID 67314578 | 10% |
Reaction Steps
A solution of 5-fluoro-1,3-dihydro-indol-2-one (75 mg, 0.49 mmol) in THF (4 mL) is treated with a solution of lithium bis(trimethylsilyl)amide (0.8 mL of a 1 M solution in THF, 0.8 mmol) dropwise. The resulting solution is stirred at room temperature for 10 min. A solution of 2-(4-hydroxy-piperidin-2-ylmethyl)-7H-furo[3,4-b]pyridin-5-one (70 mg, 0.28 mmol) in THF (2 mL) is added dropwise to the reaction mixture. The resulting solution is stirred for 6 h. The reaction mixture is treated with additional lithium bis(trimethylsilyl)amide (0.3 mL of a 1 M solution in THF, 0.3 mmol) dropwise and the reaction mixture is stirred at room temperature overnight. The reaction mixture is poured into a cold aqueous 10% HCl solution (7 mL). The resulting mixture is heated to 50° C. for 1 h and then poured into 100 mL ice water. Solid NaHCO3 is carefully added to adjust the pH to 8. The aqueous layer is extracted with EtOAc (2×). The combined organic extracts are dried with Na2SO4, filtered and concentrated. The residue is purified by chromatography (silica gel, MeOH-Chloroform). The product containing fractions are concentrated to give the title compound as a yellow solid (11 mg, 10%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977351B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-ed24629977e34ae79db183eb6eeed92c |
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| Source note | uspto-grants-2011_07 |
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