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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | Dimethylamine tetrahydrofuran | HCID 22320367 | — |
| Reactant | HCID 23155694 | HCID 23155694 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23155763 | HCID 23155763 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07799775B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-f0bcf781f46f4b0ea4541733c3dda23a |
|---|
| Source note | uspto-grants-2010_09 |
|---|