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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357566Generated: November 1, 2026

Piperazine → HCID 68455894, compound

https://huagongshe.com/reaction/2357566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromo-1-chlorophthalazineHCID 22030424—
SolventAcetonitrileHCID 6342—
ProductHCID 68455894HCID 6845589464.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 6-bromo-1-chlorophthalazine (Example 1, 0.146 g, 0.6 mmol), piperazine (0.1 g, 1.2 mmol) and potassium carbonate (0.08 g, 0.6 mmol) in 5 mL acetonitrile was added to a glass microwave reaction vessel. The reaction mixture was stirred and heated in a Smith Synthesizer® microwave reactor (Personal Chemistry, Inc., Upssala, Sweden) at 180° C. for 20 min. After about 20 min., all starting material was converted to product (M+1=293, 295). The mixture was concentrated under vacuum, and purified via flash chromatography (silica gel) eluting with a gradient of 2% 2M ammonia in MeOH/DCM to 6% 2M ammonia in MeOH/DCM to give (0.113 g) 6-bromo-1-(piperazin-1-yl)phthalazine as a yellow solid. Found MS (ES+): 293, 295(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-316b0bc0f2f34f7b9657179e2ea40d42
Source noteuspto-grants-2010_07