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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959746Generated: November 3, 2026

Stannane, tributyl(1-ethoxyethenyl)- → HCID 58190551, compound

https://huagongshe.com/reaction/1959746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
ReactantHCID 58190547HCID 58190547—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58190551HCID 58190551—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 6-(1-(6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)ethyl)-7-fluoroquinoline (100 mg, 0.305 mmol), PdCl2(PPh3)2 (21.4 mg, 0.031 mmol) and tributyl(1-ethoxyvinyl)stannane (220 mg, 0.61 mmol) in 5 mL of 1,4-dioxane was heated at 90° C. for 5 h under nitrogen. The reaction mixture was diluted with EtOAc and washed with water. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The residue was dissolved in HOAc and 3 N HCl, and stirred at rt for 3 h. The solvent was removed under reduced pressure and the residue was dissolved in DCM, washed with saturated aqueous NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel eluting with EtOAc/MeOH gradient to afford the title compound as a yellow solid. 1H-NMR (400 MHz, CDCl3) δ ppm 8.87 (d, 1H), 8.16 (d, 1H), 8.03 (d, 1H), 7.80 (d, 1H), 7.73 (d, 2H), 34 (dd, 1H), 5.39 (q, 1H), 2.62 (s, 3H), 2.09 (d, 3H). LCMS (method A): [MH]+=336, tR=4.95 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410264B2
Source datasetuspto-grants-2013_04
ORD IDord-b294867ecf8d436abf2afb8ecbfd4fd8
Source noteuspto-grants-2013_04