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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032733Generated: October 31, 2026

Ethyl Bromide → HCID 178470078, compound

https://huagongshe.com/reaction/1032733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant1-Ethyl-1,4-dihydro-4-oxo-7-(3-pyridinyl)-3-quinolinecarboxylic acidHCID 10447150—
ReactantHCID 21585181HCID 21585181—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 178470078HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959363
Source datasetuspto-grants-1990_09
ORD IDord-8e8ed2816f6840389f48f03791bd7f62
Source noteuspto-grants-1990_09