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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335855Generated: October 31, 2026

2-(Tributylstannyl)pyrazine → HCID 67382669, compound

https://huagongshe.com/reaction/335855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)pyrazineHCID 2737316—
ReactantHCID 67383557HCID 67383557—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 67382669HCID 67382669—

Reaction Conditions

Temperature110 °C

Reaction Steps

A 10 ml resealable tube was charged with tert-butyl 7′-bromo-4′-fluoro-2′-methoxy-5H-spiro[thiazole-4,9′-xanthene]-2-ylcarbamate (300 mg, 0.606 mmol), tetrakis(triphenylphosphine)palladium (70.0 mg, 0.061 mmol) and DMF (3.03 ml) and 2-(tributylstannyl)pyrazine (402 mg, 1.090 mmol). The mixture was stirred for 3 hr at 110° C. The mixture was partitioned between EtOAc and water. The organic layer was washed twice with water, filtered through celite and concentrated under reduced pressure. The solids were triturated with hexane to remove excess tin residue before being filtered. Purification by silica gel chromatography (10-80% CH2Cl2/MeOH/NH4OH in CH2Cl2) to provide tert-butyl 4′-fluoro-2′-methoxy-7′-(pyrazin-2-yl)-5H-spiro[thiazole-4,9′-xanthene]-2-ylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-9a11ced67d9b41aab0bc2cb3ce4a2767
Source noteuspto-grants-2014_11