HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Phosphate, Tribasic → 1-[(2-Cyclopropyl-4-nitrophenyl)methyl]-4-methylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 1-[(2-Bromo-4-nitrophenyl)methyl]-4-methylpiperazine | HCID 46838611 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene water | HCID 22272177 | — |
| Product | 1-[(2-Cyclopropyl-4-nitrophenyl)methyl]-4-methylpiperazine | HCID 46838612 | 96.8% |
Reaction Steps
A mixture of 1-(2-bromo-4-nitrobenzyl)-4-methylpiperazine (0.94 g, 3.0 mmol), 0.77 g (9.0 mmol) of cyclopropylboronic acid, 0.067 g (0.30 mmol) of Pd(OAc)2, 2.87 g (13.5 mmol) of K3PO4, and 0.168 g (0.60 mmol) of tricyclohexylphosphine in 18 mL of toluene/water (5:1) was heated at reflux under an atmosphere of N2 for 19 h. The reaction mixture was concentrated and the crude product was purified by silica gel chromatography (eluted with 5% MeOH/DCM; MeOH was pre-saturated with ammonia gas) to provide 0.80 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029533B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-53134630ffeb4208aca6426caa6f0491 |
| Source note | uspto-grants-2015_05 |