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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46203Generated: October 29, 2026

Tetrahydrofuran → 3-(2-Chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyl)-6-(phenylethynyl)pyridazine

https://huagongshe.com/reaction/46203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPhenylacetyleneHCID 10821—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86664426HCID 86664426—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
Product3-(2-Chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyl)-6-(phenylethynyl)pyridazineHCID 67287576—

Reaction Steps

To a mixture of Intermediate 6 (compound 24, 381 mg, 0.5 mmol), dichlorobis(triphenyl-phosphine)palladium (II) (35 mg, 0.05 mmol) and copper(I) iodide (10 mg, 0.05 mmol) in tetrahydrofuran (10 mL) was added N,N-diisopropylethylamine (0.35 mL, 2.5 mmol) and phenylacethylene (0.07 mL, 0.6 mmol). The resulting mixture was stirred at ambient temperature overnight. After dilution with ethyl acetate, the organic layer was washed with water and brine prior to drying over magnesium sulfate. Filtration through a plug of silica gel and removal of the volatiles under reduced pressure yielded titled compound as a brown solid, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541380B2
Source datasetuspto-grants-2013_09
ORD IDord-7e8229c8b0bc405aafc93935874746f9
Source noteuspto-grants-2013_09