HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169023Generated: October 25, 2026
4-Benzhydryl-1-piperazinepropanol → 6-[3-[4-(Diphenylmethyl)piperazino]propoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine dihydrochloride
https://huagongshe.com/reaction/1169023
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Benzhydryl-1-piperazinepropanol | HCID 15524146 | — |
| Reactant | 6-Chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine | HCID 22989227 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-[3-[4-(Diphenylmethyl)piperazino]propoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine dihydrochloride | HCID 22989368 | 142.7% |
Reaction Steps
4-(Diphenylmethyl)-1-piperazinepropanol (466 mg) was dissolved in dried tetrahydrofuran (10 ml), followed by addition of sodium t-butoxide (173 mg). The mixture was refluxed under heating for 30 minutes. After the mixture was cooled, 6-chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine (295 mg) was added thereto. The resulting mixture was refluxed for 3 hours under heating. After cooling, ice-water was added to the mixture, followed by extraction with ethyl acetate. The extract was washed with an aqueous sodium chloride saturated solution, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with a mixture of ethyl acetate and methanol (10:1). Fractions containing the objective compound were collected and dissolved in ethanol (10 ml), followed by addition of 1N-HCl (3 ml). The mixture was concentrated under reduced pressure. The resulting crystals were recrystallized from ethyl acetate to yield the title compound (582 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06627630B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-78d399a7f2ac435590a5d11c96adc963 |
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| Source note | uspto-grants-2003_09 |
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