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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266308Generated: November 2, 2026

TBAF tetrahydrofuran → HCID 18548957, compound

https://huagongshe.com/reaction/1266308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTBAF tetrahydrofuranHCID 11078149—
ReactantHCID 18548976HCID 18548976—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 18548957HCID 1854895745.3%

Reaction Steps

To 800 mg of 4-(3-bromo-phenylamino)-6-trimethylsilanylethynyl-[1,7]naphthyridine-3-carbonitrile in 20 mL of tetrahydrofuran at 0° C. under an inert atmosphere was added 2.5 mL of 1 M tetrabutylammonium fluoride/tetrahydrofuran. After 1 hour at ambient temperature, the reaction was diluted with ethyl acetate and washed with brine. The organic layer was dried with sodium sulfate and evaporated. The product was purified by flash chromatography on silica gel to give 300 mg of 4-(3-bromo-phenylamino)-6-ethynyl-[1,7]naphthyridine-3-carbonitrile: melting point 224° C. (decomposed); mass spectrum (m/e): M+H 349.1, 351.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548496B2
Source datasetuspto-grants-2003_04
ORD IDord-9f0b9c4eef764b91ad6fd5b9610342db
Source noteuspto-grants-2003_04