HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → HCID 178470078, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Ethyl-1,4-dihydro-4-oxo-7-(3-pyridinyl)-3-quinolinecarboxylic acid | HCID 10447150 | — |
| Reactant | HCID 21585181 | HCID 21585181 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178470078 | HCID 178470078 | — |
Reaction Steps
To a suspension of 0.53 g sodium hydride (50%) in 50 ml DMF was added 2.40 g dioxobenzoxazine from part (a). After 15 min. 1.20 g ethyl bromide was added and the mixture was stirred overnight at room temperature. Sodium hydride (1.06 g) was then added followed by 3.52 g diethyl malonate dropwise. The reaction mixture was heated on a steam bath for 2 hrs., then poured into dilute acetic acid and concentrated in vacuo. The residue was chromatographed on silica gel to give 1.35 g ethyl 1-ethyl-1,4-dihydro-2-hydroxy-4-oxo-7-(4-pyridinyl)-3quinolinecarboxylate used directly in the next reaction. A sample of the compound upon further purification was obtained as a yellow powder, m.p. 153-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959363 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-8e8ed2816f6840389f48f03791bd7f62 |
| Source note | uspto-grants-1990_09 |