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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | HCID 14626316 | HCID 14626316 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-[3-[4-(Carbomethoxymethoxy)phenethylamino]-2-hydroxypropoxy]flavone Maleate | HCID 14626319 | 10% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04889941 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-dc6241a72ce440c2b3f8362577e595a0 |
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| Source note | uspto-grants-1989_12 |
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