Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897317Generated: November 1, 2026

Trifluoroacetic acid → HCID 20816856, compound

https://huagongshe.com/reaction/897317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-PropanesultamHCID 642157—
Reactant5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamideHCID 22346401—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
ProductHCID 20816856HCID 20816856—

Reaction Steps

A mixture of 1,3 propanesultam (prepared as in White et al, J. Org Chem. 1987, 52: 2162) (0.081 g, 0.66 mmol), 5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide (0.10 g, 0.27 mmol), potassium carbonate (0.092 g, 0.66 mmol) and copper powder (0.017 g, 0.27 mmol) under an atmosphere of argon was stirred at 160C for 16 hr. The reaction was allowed to cool to room temperature and the residue was treated with DMF (5 mL) and TFA (1.5 mL) and filtered through a pad of celite to remove the solids. The filtrate was purified by reverse phase HPLC. (Waters PrePak 500 cartridge C18, Gradient elution with Water:Acetonitrile 95:5 to 5:95 with 0.1% TFA at 75 mL/min over 45 mins). Lyophilization of the pure fractions afforded the title compound as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-82f62c54d58843a0a54b4abb7ae6b40d
Source noteuspto-grants-2005_07