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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507454Generated: November 2, 2026

Tributylstannane → HCID 117701723, compound

https://huagongshe.com/reaction/1507454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHCID 117701561HCID 117701561—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117701723HCID 11770172395%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221811B2
Source datasetuspto-grants-2015_12
ORD IDord-ecf39e04c44d4584801fa8afa8913497
Source noteuspto-grants-2015_12