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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478082Generated: October 31, 2026

Water → 7-[3-[4-(Carbomethoxymethoxy)phenethylamino]-2-hydroxypropoxy]flavone Maleate

https://huagongshe.com/reaction/478082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethyl bromoacetateHCID 60984—
ReactantHCID 14626316HCID 14626316—
SolventDimethylformamideHCID 6228—
Product7-[3-[4-(Carbomethoxymethoxy)phenethylamino]-2-hydroxypropoxy]flavone MaleateHCID 1462631910%

Reaction Conditions

Temperature-20 °C

Reaction Steps

7-[3-[(4-Hydroxyphenethyl)amino]-2-hydroxypropoxy]flavone (10.8 g, 25.1 mmol), Example 13, was dissolved in 20 ml of warm DMF at 50°-60° C. and then cooled to -20° C. Sodium hydride (1.2 g, 0.0251 mmol) was added portionwise to the above cooled solution, stirred at -20° C. for 1 hour, and then cooled to -40° C. Methyl bromoacetate (3.8 g, 25.1 mmol) was added dropwise to the stirred solution and the reaction mixture was kept at this temperature for 2 hours and at RT overnight. The reaction was poured into 1.5 l of water, the water decanted, and the residue washed with two portions of water. The gummy material was then purified by flash column chromatography, eluting with CHCl3 --MeOH (20:1). The isolated material (2.7 g) was recrystallized from methanol, and the crystallized solid was treated with 30 ml of ethanol and maleic acid (0.3 g) to give the title compound as white crystals, mp 154°-156° C., 1.5 g (10% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04889941
Source datasetuspto-grants-1989_12
ORD IDord-dc6241a72ce440c2b3f8362577e595a0
Source noteuspto-grants-1989_12