HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 3-methoxy-1,7-naphthyridin-8(7H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-(2,2-Dimethoxyethyl)-5-methoxypicolinamide | HCID 86732286 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-methoxy-1,7-naphthyridin-8(7H)-one | HCID 86732288 | 92% |
Reaction Steps
To a mixture of 3-(2,2-dimethoxyethyl)-5-methoxypicolinamide (6.74 g, 28.1 mmol) in toluene (112 ml) was added 4-methylbenzene sulfonic acid (monohydrate; 0.534 g, 2.81 mmol). The reaction mixture was heated to reflux for 20 h. The reaction mixture was cooled to rt and concentrated in vacuo to a volume of ca. 15 mL. The residue was triturated with heptanes and filtered to afford 3-methoxy-1,7-naphthyridin-8(7H)-one (4.53 g, 25.7 mmol, 92% yield) as a crude, tan solid that was advanced without further purification. Crude LCMS showed complete conversion to product MS m/z=177.1 [M+H]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296734B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-2835b9766c7c447684a9e641688e64ff |
| Source note | uspto-grants-2016_03 |