HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897350Generated: October 29, 2026
HCID 22346271, compound → HCID 20816883, compound
https://huagongshe.com/reaction/897350
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22346271 | HCID 22346271 | — |
| Reactant | 5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide | HCID 22346401 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20816883 | HCID 20816883 | — |
Reaction Steps
To a solution of 5-bromo-N-(4-fluorobenzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide (0.147 g, 0.39 mmol), 5-(methylsulfonyl)-1,2,5-thiadiazepane 1,1-dioxide (0.081 g, 0.355 mmol) and Cu2O (0.056 g, 0.39 mmol) in pyridine (2.4 mL) were heated at reflux for 16 hr. The reaction was filtered and the solids washed with CHCl3 (100 mL). The filtrate was stirred for 1 hr with disodium ethylenediamine tetraacetate (0.2 g in water 10 mL) in the presence of air. The organic extracts were stirred for 1 hr with disodium ethylenediamine tetraacetate (0.2 g in water 10mL) in the presence of air. The organic extracts were dried (MgSO4) and the solvent evaporated in vacuo. The residue was 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% TFA) at 15 ml/min) to afford the title compound after lyophilization.
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-c1d575fac5f2467ca824efa18f424c5c |
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| Source note | uspto-grants-2005_07 |
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