HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 178437756, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-Amino-3-quinolinecarboxamide | HCID 5200228 | — |
| Solvent | Ethyl orthopropionate | HCID 66995 | — |
| Product | HCID 178437756 | HCID 178437756 | 236.5% |
Reaction Steps
A slurry of 2-aminoquinoline-3-carboxamide (1.0 g, 5.3 mmol), (Campaigne, E.; Randau, G. J. Het. Chem. 1971, Vol. 8, p. 111) and p-toluenesulfonic acid-monohydrate (50 mg) in triethyl orthopropionate (25 mL) was refluxed for 24 hours. After cooling, the reaction mixture was diluted into diethyl ether (50 mL), the resulting solids filtered and washed with diethyl ether. The solids were recrystallized from formamide to afford 0.14 g of the title compound; m.p. 240-245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05908930 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-77e6701bec1f45ec93bb900ec1b7b13e |
| Source note | uspto-grants-1999_06 |