Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357575Generated: November 1, 2026

Potassium Carbonate → 2-(6-Bromophthalazin-1-yl)-5-isopropyl-2,5-diaza-bicyclo[2.2.1]heptane

https://huagongshe.com/reaction/2357575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromo-1-chlorophthalazineHCID 22030424—
Reactant2-Isopropyl-2,5-diazabicyclo[2.2.1]heptane dihydrochlorideHCID 68456075—
SolventAcetonitrileHCID 6342—
Product2-(6-Bromophthalazin-1-yl)-5-isopropyl-2,5-diaza-bicyclo[2.2.1]heptaneHCID 6845497846.7%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 6-bromo-1-chlorophthalazine (Example 1, 90 mg, 370 μmol), 2-isopropyl-2,5-diaza-bicyclo[2.2.1]heptane dihydrochloride (95 mg, 444 μmol) and potassium carbonate (153 mg, 1109 μmol) in 10 mL acetonitrile was stirred at 130° C. under in a sealed tube. The mixture turned red in about 5 min. The reaction was monitored by MS. After about 1 h at 130° C., MS and TLC showed all starting material was converted to product (M+1=347, 349). The mixture was cooled down to room temperature, and concentrated on a Rotavaporator. After purification by column (eluting with gradient of 2-10% 2M ammonia in methanol to DCM), 2-(6-bromophthalazin-1-yl)-5-isopropyl-2,5-diaza-bicyclo[2.2.1]heptane (60 mg) was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-fd80c4107ed34b238a174c7c744eabdc
Source noteuspto-grants-2010_07