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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897336Generated: October 30, 2026

Ethylenediaminetetraacetic Acid → HCID 20816879, compound

https://huagongshe.com/reaction/897336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediaminetetraacetic AcidHCID 6049—
ReactantDisodiumHCID 141233—
Reactant5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamideHCID 22346401—
ReactantHCID 22346408HCID 22346408—
CatalystHCID 178419072HCID 178419072—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
ProductHCID 20816879HCID 20816879—

Reaction Conditions

Temperature115 °C

Reaction Steps

A mixture of 5-bromo-N-(4-fluorobenzyl)-8-hydroxy[1,6]naphthyridine-7-carboxamide (0.99 g, 2.66 mmol), 1,2,5-thiadiazepan-4-one 1,1-dioxide from step 2 (0.41 g, 2.5 mmol) and copper (I) oxide (0.18 g, 1.25 mmol) in pyridine (13 mL) was heated in an oil bath at 115° C. overnight. The resultant mixture was treated with a mixture of chloroform (200 mL) and a saturated aqueous solution of ethylenediamine tetraacetic acid, disodium salt (200 mL) and stirred vigorously at room temp overnight in the presence of air. The slurry was filtered through a pad of Celite. The organic extract was separated, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The residue was dissolved in DMSO and subjected to HPLC purification on C-18 stationary phase eluted with water/acetonitrile/TFA mobile phase. Collection and lyophilization of appropriate fractions provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-e0e29a9bc6604ec49c54c0a74c8301aa
Source noteuspto-grants-2005_07