HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067496Generated: October 26, 2026
Diisopropylethylamine → 6-[4-[4-(Diphenylmethoxy)piperidino]butylamino][1,2,4]triazolo[1,5-b]pyridazine
https://huagongshe.com/reaction/1067496
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-(1,2,4)triazolo(1,5-b)pyridazine | HCID 11240611 | — |
| Reactant | 1-Piperidinebutanamine, 4-(diphenylmethoxy)- | HCID 11739259 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 6-[4-[4-(Diphenylmethoxy)piperidino]butylamino][1,2,4]triazolo[1,5-b]pyridazine | HCID 11004976 | 9.1% |
Reaction Steps
4-(Diphenylmethoxy)-1-piperidinebutanamine (1.83 g) and 6-chloro[1,2,4]triazolo[1,5-b]pyridazine (557 mg) were dissolved in n-butanol (30 ml), followed by addition of N-ethyldiisopropylamine (931 mg). The mixture was refluxed under heating for 14 hours. After being cooled, the mixture was concentrated under reduced pressure, followed by addition of ice-water and extraction with ethyl acetate. The extract was washed with an aqueous sodium chloride saturated solution, dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to a silica-gel column chromatography and eluted with a mixture of ethyl acetate, methanol and triethylamine (45:5:1). Fractions containing the objective compound were collected and concentrated. The resulting crystals were collected, washed with ethylether and dried to yield the title compound (149 mg).
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-b9865e2c56ce4edcb9f3ddac547eb90e |
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| Source note | uspto-grants-2001_06 |
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