HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 1-(4-1H-indolyl)-4-[3,3-bis-(2-pyridyl)propyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(piperazin-1-yl)-1H-indole | HCID 594590 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3,3-Bis-(2-pyridyl)propionaldehyde | HCID 22482105 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-1H-indolyl)-4-[3,3-bis-(2-pyridyl)propyl]piperazine | HCID 22482108 | 13% |
Reaction Steps
A mixture of 1.15 g of Compound 16B, 1.2 g of 1-(4-indolyl)piperazine (prepared as described in EP 138,280), 1.24 mL of acetic acid, 1.71 g of sodium triacetoxyborohydride and 85 mL of 1,2-dichloroethane was stirred at room temperature for 24 h. Afterwards it was diluted with water and alkalinized with sodium carbonate. The organic layer was dried on sodium sulphate and evaporated to dryness affording 1.53 g of crude, which was purified by flash chromatography (ethyl acetate-2.2 N methanolic ammonia, gradient from 9.4:0.6 to 9.2:0.8) affording 0.28 g (13%) of the title product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06894052B1 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-db0f40ea5c0a4605b13a3af8ae4a87b1 |
| Source note | uspto-grants-2005_05 |