HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → HCID 19436809, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Chloro-5-methoxypyridazine | HCID 10975612 | — |
| Reactant | HCID 178481858 | HCID 178481858 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 19436809 | HCID 19436809 | — |
Reaction Steps
1-Methyl-3-(pentafluoroethyl)-1H-pyrazol-5-ol (0.44 g, 0.002 mole), 3-chloro-5-methoxypyridazine (0.29 g, 0.002 mole), and 2,6-lutidine (0.27 g, 0.0024 mole) were refluxed under N2 in toluene (8 mL) for 15 h. This mixture was poured into ethyl acetate and washed with 7% HCl, water and then with saturated sodium bicarbonate. The organic layer was dried (MgSO4), filtered through silica gel with ethyl acetate, and evaporated in vacuo to give 5-methoxy-3-[[1-methyl-3-(pentafluoroethyl)-1H-pyrazol-5-yl]oxy]pyridazine as a light yellow solid. The compound was recrystallized to give (0.45 g, 69% yield) Compound 18, a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05536701 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-a16259c0ac4643e399bf3b455fc4feeb |
| Source note | uspto-grants-1996_07 |