HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 117701723, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 117701561 | HCID 117701561 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117701723 | HCID 117701723 | 95% |
Reaction Steps
Tri-n-butyltin hydride (104 μL, 0.39 mmol) and a catalytic amount of azobisisobutyronitrile were added to a solution of benzyl 4-[7-(benzyloxy)-3-methyl-4-oxo-8-{2,2,2-trifluoro-1-[(1H-imidazol-1-ylcarbonothioyl)oxy]ethyl}-4H-chromen-2-yl]piperidine-1-carboxylate (135 mg, 0.20 mmol) obtained in Example 36-3 in tetrahydrofuran (1.5 mL), and the mixture was heated to reflux for 1 hour. The reaction solution was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=80/20→40/60) to obtain 105 mg of the title compound (yield: 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221811B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-ecf39e04c44d4584801fa8afa8913497 |
| Source note | uspto-grants-2015_12 |