HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397578Generated: October 29, 2026
Ethyl bromoacetate → HCID 23000308, compound
https://huagongshe.com/reaction/397578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 23000323 | HCID 23000323 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23000308 | HCID 23000308 | — |
Reaction Steps
0.459 g of 6-(3-[4-(diphenylmethoxy)piperidino]propoxy][1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one was suspended in 6 ml of N,N-dimethylformamide; 0.048 g of 60% oily sodium hydride was added, followed by stirring at room temperature for 1 hour. Under ice cooling, 0.133 ml of ethyl bromoacetate was added, followed by stirring at room temperature for 4 hours. After ice water was added, the reaction mixture was extracted with ethyl acetate; the extract was washed with saturated saline and dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate-methanol-triethylamine (185:15:2). The desired fraction was collected and concentrated; the crystal obtained was filtered, washed with diethyl ether, and dried, to yield 0.235 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610694B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-84a4a20907b34b018214de7020a3515b |
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| Source note | uspto-grants-2003_08 |
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