HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369448Generated: October 30, 2026
Water → 3-(2-Fluorophenyl)-6-(2-Methyl-2H-1,2,4-Triazol-3-Ylmethoxy)-7-(3-Oxocyclobutyl)-1,2,4-Triazolo[4,3-b]Pyridazine
https://huagongshe.com/reaction/1369448
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Chromic Acid | HCID 24425 | — |
| Reactant | 3-(2-Fluorophenyl)-7-(3-hydroxycyclobutyl)-1,2,4-triazolo[4,3-b]pyridazin-6-one | HCID 22609891 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(2-Fluorophenyl)-6-(2-Methyl-2H-1,2,4-Triazol-3-Ylmethoxy)-7-(3-Oxocyclobutyl)-1,2,4-Triazolo[4,3-b]Pyridazine | HCID 22609920 | — |
Reaction Steps
8N Chromic acid was added to a solution of 3-(2-fluorophenyl)-7-(3-hydroxycyclobutyl)-1,2,4-triazolo[4,3-b]pyridazin-6-one (0.36 g, 1.2 mmol) in acetone (50 ml) dropwise, until excess was present (red colour remained). The reaction was then stirred for 2 hours before isopropanol was added until the blue colour remained and no excess chromic acid was present. Water (50 ml) was added and the aqueous layer extracted with ethyl acetate (4×50 ml), organic layers were combined, washed with brine (50 ml), dried (MgSO4), filtered and concentrated to give the desired product as a white solid. Data for the title compound: 1H NMR (360 MHz, DMSO) δ3.41 (2H, s), 3.43 (2H, s), 3.73-3.78 (1H, m), 7.42-7.50 (2H, m), 7.64-7.72 (1H, m), 7.83-7.88 (1H, m), 8.38 (1H, s); MS (ES+) m/e 299 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06579875B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-ed0ed63cae094c69a1a0a46b18685bf8 |
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| Source note | uspto-grants-2003_06 |
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