HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 67746822, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 2-(4-bromophenyl)-1H-benzimidazole | HCID 286182 | — |
| Reactant | HCID 18993040 | HCID 18993040 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ammonia | HCID 222 | — |
| Product | HCID 67746822 | HCID 67746822 | 30.4% |
Reaction Steps
A mixture of 2-(4-bromophenyl)-1H-benzimidazole (Example F) (8.08 g), 1-but-3-enyl-4-phenylpiperazine (Example G) (8.0 g), palladium acetate (0.66 g), tri-o-tolylphosphine (1.8 g) and triethylamine (7.05 g) in acetonitrile (100 mL) is stirred at reflux for 2 hours. The mixture is cooled and filtered through Celite. The filtrate is evaporated to leave a brown solid. This solid is purified by MPLC on silica gel eluting with 100:8:1 dichloromethane: ethanol: 0.880 aqueous ammonia to give 1.84 g of the title compound as a white solid; mp 140°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05486517 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-58e9532f1c9a4e5fb612bfaaf26b7ec6 |
| Source note | uspto-grants-1996_01 |