HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 6-chloro-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Chloro-4-hydrazinophthalazine | HCID 2793752 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 6-chloro-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine | HCID 1502563 | 74.1% |
Reaction Steps
128 μl (1.1 mmol) of benzoyl chloride was added to a xylene solution (10 ml) of 194 mg (1.0 mmol) of (4-chloro-phthalazin-1-yl)-hydrazine and 182 μl (1.3 mmol) of triethylamine, and stirred overnight under reflux. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction liquid, and extracted with chloroform. The organic layer was washed with saturated saline solution, dried and concentrated under reduced pressure to obtain 208 mg (yield: 74%) of 6-chloro-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645756B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-5d343d23d5e34915aaa5227b073c0434 |
| Source note | uspto-grants-2010_01 |