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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714801Generated: October 30, 2026

2-(Di-tert-butylphosphino)biphenyl → HCID 23155763, compound

https://huagongshe.com/reaction/1714801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantDimethylamine tetrahydrofuranHCID 22320367—
ReactantHCID 23155694HCID 23155694—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23155763HCID 2315576325%

Reaction Conditions

Temperature80 °C

Reaction Steps

After dissolving 1.01 g of 1-(4-benzylpiperazin-1-yl)-7-chloroisoquinoline as synthesized in above Step 1 in 30 ml of tetrahydrofuran, 20 mg of palladium acetate, 48 mg of 2-(di-tert-butylphosphino)biphenyl, 450 mg of sodium-tert-butoxide and 5 ml of 2.0 M dimethylamine-tetrahydrofuran solution were added to the solution and sealed in a tube. This mixture was stirred at 80° C. for 16 hours. Removing the insoluble matter by filtration, the solvent was distilled off under reduced pressure and the residue was purified on silica gel column chromatography (methanol:chloroform=1:19) to provide 261 mg (25%) of 1-(4-benzylpiperazin-1-yl)-7-dimethylaminoisoquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799775B2
Source datasetuspto-grants-2010_09
ORD IDord-f0bcf781f46f4b0ea4541733c3dda23a
Source noteuspto-grants-2010_09