HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517809Generated: October 25, 2026
Potassium Carbonate → 3-Chloro-6-(oxetan-2-ylmethoxy)[1,2,4]triazolo[4,3-b]pyridazine
https://huagongshe.com/reaction/517809
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine | HCID 1482346 | — |
| Reactant | (Oxetan-2-yl)methanol | HCID 12284142 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Chloro-6-(oxetan-2-ylmethoxy)[1,2,4]triazolo[4,3-b]pyridazine | HCID 67524580 | — |
Reaction Steps
a mixture of 756 mg of commercial 3,6-dichloro[1,2,4]triazolo[4,3-b]pyridazine, 0.352 cm3 of 2-hydroxymethyloxetane and 552 mg of potassium carbonate in 8 cm3 of N,N-dimethylformamide is heated at 100° C. for 6 h and then stirred at 20° C. overnight. The reaction medium is concentrated to dryness under vacuum. The residue obtained is purified by chromatography on a Merck cartridge of 25 g of silica 15-40 μm by solid deposit, elution being carried out with a dichloromethane/methanol gradient of 100/0 to 97/03. 701 mg of 3-chloro-6-(oxetan-2-ylmethoxy)[1,2,4]triazolo[4,3-b]pyridazine are thus obtained in the form of a beige solid, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115134B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-0cf7bdb542bd42b9958625e0d297b56a |
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| Source note | uspto-grants-2015_08 |
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