Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897283Generated: October 29, 2026

Piperazine → HCID 10137646, compound

https://huagongshe.com/reaction/897283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 10180885HCID 10180885—
SolventDimethylformamideHCID 6228—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 10137646HCID 10137646—
ProductHCID 21903395HCID 21903395—

Reaction Steps

To a solution of 5-bromo-N-(3,5-dichlorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide from Example 50 (25 mg, 0.060 mmol), piperazine (30.25 mg, 0.35 mmol) in 1-methylpyrrolidinone (0.25 ml) was heated at 135 C for 18 hrs. The resulting mixture was further diluted with DMF (0.25 ml) and TFA (50 ul) and purified by preparative HPLC (Gilson Semi Preparative HPLC System and a YMC Combiprep Pro Column (50×20 mm i.d., C18, S-5 um, 120A) eluting with 5-95% acetonitrile/water (0.1%) at 15 ml/min) to afford the title compound as the piperazin-4-ium trifluoroacetate salt after lyophillization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-c0f7b38bb472415098d3ddfca6b20188
Source noteuspto-grants-2005_07