Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897313Generated: October 27, 2026

N-BOC-ethylenediamine → HCID 86587464, compound

https://huagongshe.com/reaction/897313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BOC-ethylenediamineHCID 187201—
Reactant5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamideHCID 22346401—
ReactantTri(butyl)vinyltinHCID 53438229—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86587464HCID 86587464—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromo-N-(4-fluorobenzyl)-8-hydroxy-[1,6]naphthyridine-7-carboxamide (2.00 g, 5.33 mmol), tri-n-butylvinyl tin (3.12 mL, 10.70 mmol), bis (triphenylphosphine)palladium(II) chloride (0.75 g, 1.10 mmol), N-Boc-ethylenediamine (4.23 g, 26.6 mmol) in dioxane (50 mL) was purged with nitrogen and heated with stirring at 100° C. in a sealed tube overnight. The resultant product mixture was filtered through a pad of Celite. The filtrate was 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 N-Boc amino napthyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-2bb9974aaf434529984fa2460dd7142d
Source noteuspto-grants-2005_07