HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 21711192, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21711196 | HCID 21711196 | — |
| Product | HCID 21711192 | HCID 21711192 | — |
Reaction Steps
A mixture of 1,2-dihydro-5-(2-thienyl)-2-oxo-1,6-naphthyridine-3-carbonitrile (10.0 g), ethanol (300 ml) and 10N NaOH (300 ml) was refluxed overnight. After cooling, the reaction mixture was neutralized with acetic acid, and the precipitated crystals were separated by filtration, washed with water, isopropanol and diisopropyl ether in this order and then dried to give the title compound (Compound No. 44)(10.5 g) as pale yellow crystals. M.p. 278° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172079B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-d3f18e7c9a0141548cc2758deabcfca2 |
| Source note | uspto-grants-2001_01 |