HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 18999734, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-1-propanol | HCID 12313 | — |
| Reactant | Desmethylmianserin | HCID 115194 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18999734 | HCID 18999734 | — |
Reaction Steps
1.5 g of 1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepine, 0.74 g of 3-chloropropanol, 2.32 g of potassium carbonate and 0.10 g of sodium iodide were added to 30 ml of ethanol, and the mixture was heated under reflux for 20 hours. At the end of this time, the reaction mixture was filtered, and then The solvent was removed from the filtrate by distillation under reduced pressure. The residue was then subjected to column chromatography through silica gel, and the desired compound was obtained as crystals from the fractions eluted with 5% by volume ethanol in chloroform; it was then recrystallized from ethyl acetate, to afford 1.28 g (69% yield) of the title compound, melting at 127°-128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05461051 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-72765de7217c49f2b5dc0a4b5ac5123f |
| Source note | uspto-grants-1995_10 |