HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569969Generated: October 30, 2026
Ethyl bromoacetate → HCID 12899521, compound
https://huagongshe.com/reaction/569969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 14128502 | HCID 14128502 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12899521 | HCID 12899521 | — |
Reaction Steps
20 Grams of 5-(3-piperazinylpropoxy)-3,4-dihydrocarbostyril and 3 ml of ethyl 2-bromoacetate and 1.5 ml of triethylamine are mixed with 20 ml of dimethyl formamide at 50°-60° C. for 8 hours under stirring conditions. The reaction mixture is concentrated under reduced pressure and to the viscous residue thus obtained are added 30 ml of 2% sodium hydrogencarbonate aqueous solution followed by extraction with chloroform. The chloroform layer is washed with water, dried and chloroform is removed by distillation. The residue is purified by silica gel chromatography and recrystallized from isopropanol to obtain 5-{3-[4-(2-acetyloxyethyl)piperazinyl]propoxy}-3,4-dihydrocarbostyril in the form of colorless needle-like crystals with a melting point of 131°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04734416 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-04326ee31ad5401498f619d3202258ed |
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| Source note | uspto-grants-1988_03 |
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