HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 11857307, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylpyrrolidine | HCID 13003 | — |
| Reactant | HCID 59457464 | HCID 59457464 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11857307 | HCID 11857307 | 42% |
Reaction Steps
A mixture of 4-(chloromethyl)-2-[4-(3-chloropropoxy)phenyl]-1,3-oxazole ax57 (0.172 g, 0.6 mmol, 1 eq), sodium iodide (0.018 g, 0.12 mmol, 0.2 eq), potassium carbonate (0.373 g, 2.7 mmol, 4.5 eq) and 2-methylpyrrolidine in acetonitrile (5 ml) is stirred at room temperature for 72 h. Piperidine (0.05 g, 0.6 mmol, 1 eq) is then added and the mixture is stirred at 80° C. overnight. The volatiles are then removed under vacuum and the residue is purified by chromatography (dichloromethane/methanol/ammonia 96:3.6:0.4) to give 1-[3-(4-{4-[(2-methylpyrrolidin-1-yl)methyl]-1,3-oxazol-2-yl}phenoxy)propyl]piperidine 30 as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790720B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-994709cefe2e484299756834d120dab5 |
| Source note | uspto-grants-2010_09 |