HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 70247622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 70243410 | HCID 70243410 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70247622 | HCID 70247622 | — |
Reaction Steps
A solution of 0.675 g (1.756 mM) of (E)-1-(piperidin-4-yl)-3-(5-thia-1,8b-diazaacenaphthylen-4-yl)propen-1-one dihydrochloride, 0.52 g (2.63 mM) of 1-bromo-3-phenylpropane, and 0.86 ml (6.15 mM) of triethylamine in 30 ml of acetonitrile, and the mixture was refluxed for 1 day. This reaction mixture was poured in aqueous solution of sodium hydrogen carbonate and extracted with 3 portions of ethyl acetate. The organic layers were pooled and dried over MgSO4 and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate˜ethyl acetate/methanol: 4/1) to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235731B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-c2a3a90d5c934b4aa9e5b42ede7b5e60 |
| Source note | uspto-grants-2001_05 |