Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | ETHYL 4-OXO-1,4-DIHYDROPYRROLO[1,2-B]PYRIDAZINE-3-CARBOXYLATE | HCID 10104421 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Pyrrolo[1,2-b]pyridazin-4(1H)-one | HCID 57415871 | 67.1% |
Reaction Steps
A mixture of ethyl 4-oxo-1,4-dihydropyrrolo[1,2-b]pyridazine-3-carboxylate (206 mg, 1.0 mmol), NaCl (64 mg, 1.1 mmol), water (0.054 mL, 3.0 mmol) and DMSO (2 mL) was heated at 150° C. for 3 hours. At the end of the reaction DMSO was distilled off and the residue was purified by silica gel flash chromatography (eluted with 1-10% EtOAc/CH2Cl2) to give the title compound (90 mg, 67%) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439246B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-433b315bf8df484693d91ac2f49dc1fb |
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| Source note | uspto-grants-2008_10 |
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