Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897329Generated: October 30, 2026

Ethylenediamine → HCID 22346473, compound

https://huagongshe.com/reaction/897329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantTrifluoroacetic acidHCID 6422—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamideHCID 22346401—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 22346473HCID 22346473—

Reaction Steps

A solution of 5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide (0.21 g, 0.55 mmol), ethylene diamine (0.14 mL, 1.67 mmol) and diisopropylethylamine (0.29 mL, 1.67 mmol) in DMPU (2.0 mL) were heated at 140 C for 16 hr. Ethylene diamine (0.14 mL, 1.67 mmol) was added and the reaction heated at 140 C for a further 24 hr. The reaction was cooled to room temperature, and treated with carbonyldiimidazole (0.188 g 1.16 mmol) and diisopropylethylamine (0.29 mL, 1.67 mmol) and then heated at 120 C for 1 hr. The reaction was cooled to room temperature, acidified by the addition of TFA (0.5 mL) and 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-01e01da38de84277a0945522da7d9870
Source noteuspto-grants-2005_07