HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897313Generated: October 27, 2026
N-BOC-ethylenediamine → HCID 86587464, compound
https://huagongshe.com/reaction/897313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | 5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide | HCID 22346401 | — |
| Reactant | Tri(butyl)vinyltin | HCID 53438229 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86587464 | HCID 86587464 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921759B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-2bb9974aaf434529984fa2460dd7142d |
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| Source note | uspto-grants-2005_07 |
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