HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 59436266, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 1481283 | HCID 1481283 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59436266 | HCID 59436266 | 58.1% |
Reaction Steps
A solution of 4-oxo-N-phenyl-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxamide (0.153 g, 0.426 mmol), 1H-benzo[d][1,2,3]triazole (0.201 g, 1.69 mmol) and thionyl chloride (0.06 mL, 0.82 mmol) in methylene chloride (2 mL) was heated under microwave heating conditions at 80 watts of power for 10 min. After that time, the reaction was concentrated and the crude product purified by flash column chromatography (silica gel, hexanes to ethyl acetate) to give 0.114 g (58%) of 3-[1H-benzotriazol-1-yl(phenylimino)methyl]-1-[3-(trifluoromethyl)phenyl]pyridazin-4(1H)-one as a pale red solid that was used without further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513251B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-41ab349bc7ed430d826ca4a6d5e6f10c |
| Source note | uspto-grants-2013_08 |