Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10180885 | HCID 10180885 | — |
| Product | HCID 10115217 | HCID 10115217 | — |
Reaction Steps
To a 5 mL pyrex pressure vessel with a stirring bar was added 5-bromo-8-hydroxy-[1,6]naphthyridine-7-carboxylic acid 3,5-dichloro-benzylamide (0.055 g, 0.13 mmol), thiophenol (0.056 g, 0.50 mmol) and triethylamine (0.28 mL, 2.00 mmol). The vessel was sealed under nitrogen and the stirred mixture heated in a 135° C. oil bath for 24 h. The cooled reaction mixture was concentrated in vacuo and the residue was chromatographed on silica gel (15 g) using methanol:chloroform (5:95) as eluant to give 8-hydroxy-5-phenylsulfanyl-[1,6]naphthyridine-7-carboxylic acid 3,5-dichlorobenzylamide as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06921759B2 |
|---|
| Source dataset | uspto-grants-2005_07 |
|---|
| ORD ID | ord-4c1fa22ee4954908aec46973d8105727 |
|---|
| Source note | uspto-grants-2005_07 |
|---|