Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990778Generated: October 31, 2026

Benzoyl chloride → 6-chloro-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine

https://huagongshe.com/reaction/1990778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Chloro-4-hydrazinophthalazineHCID 2793752—
SolventO-XyleneHCID 7237—
Product6-chloro-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazineHCID 150256374.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645756B2
Source datasetuspto-grants-2010_01
ORD IDord-5d343d23d5e34915aaa5227b073c0434
Source noteuspto-grants-2010_01