HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → 6-(4-Methoxyphenyl)-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | 1-Chloro-4-(4-methoxyphenyl)phthalazine | HCID 2772390 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(4-Methoxyphenyl)-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine | HCID 1980630 | 99.3% |
Reaction Steps
163 mg (1.2 mmol) of benzohydrazide and 165 mg (1.2 mmol) of triethylamine hydrochloride were added to a xylene solution (5 ml) of 271 mg (1.0 mmol) of the obtained 1-chloro-4-(4-methoxyphenyl)-phthalazine, and then stirred under reflux for 2 hours. Water was added to the reaction liquid, extracted with ethyl acetate, and the organic layer was washed with saturated saline water. This was dried with anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 350 mg of a crude product of 6-(4-methoxyphenyl)-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645756B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-99c7ea2fee2d44129dd0051ae79afdc9 |
| Source note | uspto-grants-2010_01 |