HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-(3-Hydroxy-benzofuran-2-sulfonyl)-2H-pyridazin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Methoxy-6-(3-hydroxy-benzofuran-2-sulfonyl)-pyridazine | HCID 12071765 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-(3-Hydroxy-benzofuran-2-sulfonyl)-2H-pyridazin-3-one | HCID 12071766 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A mixture of 3-methoxy-6-(3-hydroxy-benzofuran-2-sulfonyl)-pyridazine (2.7 mmol, 820 mg), conc. HCl (2 mL), and dioxane (10 mL) was heated at 100° C. for 2 hours. The reaction mixture was cooled and evaporated to dryness. The dried residue was extracted with EtOAc (2×20 mL). The extract was dried, filtered, and the filtrate was evaporated to a residue, which was purified by silica gel chromatography (eluent:EtOAc:n-hexanes::3:1), triturated with water (10 mL), and filtered to obtain the desired product: 6-(3-hydroxy-benzofuran-2-sulfonyl)-2H-pyridazin-3-one (35%, 284 mg); mp 186° C.-189° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06849629B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-bd0ac02aa2a14ceeb9549e3b164b7d05 |
| Source note | uspto-grants-2005_02 |