Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazine | HCID 11805158 | — |
| Reactant | HCID 22989379 | HCID 22989379 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22989387 | HCID 22989387 | 64.4% |
Reaction Steps
190 mg of 60% sodium hydride in oil was suspended in 15 ml of tetrahydrofuran; 1.47 g of 4-(diphenylmethoxy)-1-[2-(2-hydroxyethoxy)ethyl]piperidine was added, followed by heating and refluxing for 1 hour. After cooling, 660 mg of 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 3 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 ethyl acetate-methanol (10:1). The desired fraction was collected; the crystal precipitated was collected by filtration, washed with ethyl ether and dried to yield 1.23 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-2b9aa6e5a7de48b8a5d0a7f58bf95896 |
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| Source note | uspto-grants-2001_06 |
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