HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067512Generated: October 26, 2026
Sodium hydride → 6-[2-[2-[4-(Diphenylmethyl)piperazino]ethoxy] ethoxy][1,2,4]triazolo[1,5-b]pyridazine dihydrochloride
https://huagongshe.com/reaction/1067512
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Decloxizine | HCID 71135 | — |
| Reactant | 6-Chloro-(1,2,4)triazolo(1,5-b)pyridazine | HCID 11240611 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-[2-[2-[4-(Diphenylmethyl)piperazino]ethoxy] ethoxy][1,2,4]triazolo[1,5-b]pyridazine dihydrochloride | HCID 22989414 | 157% |
Reaction Steps
100 mg of 60% sodium hydride in oil was suspended in 20 ml of tetrahydrofuran; 470 mg of 4-(diphenylmethyl)-1-[2-(2-hydroxyethoxy)ethyl]piperazine was added, followed by heating and refluxing for 1 hour. After cooling, 200 mg of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 4.5 hours. After cooling, ice water was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. After the dry product was concentrated under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with dichloromethane-ethyl acetate-methanol (10:10:1). The desired fraction was collected and dissolved in 5 ml of ethyl acetate; 0.83 ml of a 4 N hydrogen chloride solution in ethyl acetate was added; the crystal precipitated was collected by filtration, washed with ethyl ether and dried to yield 0.54 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248740B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-d09406e9a40245e086862f96d16a6045 |
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| Source note | uspto-grants-2001_06 |
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