HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096252Generated: October 26, 2026
Sodium hydride → 3-Methyl-1-(3-piperidin-1-yl-propyl)-4-(3-trifluoromethoxy-phenyl)-piperazin-2-one
https://huagongshe.com/reaction/1096252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(3-chloropropyl)piperidine hydrochloride | HCID 79624 | — |
| Reactant | Piperidine, 1-(3-chloropropyl)- | HCID 79625 | — |
| Reactant | 3-Methyl-4-(3-trifluoromethoxy-phenyl)-piperazin-2-one | HCID 66783006 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-Methyl-1-(3-piperidin-1-yl-propyl)-4-(3-trifluoromethoxy-phenyl)-piperazin-2-one | HCID 59159263 | 84% |
Reaction Steps
NaH (55% dispersion in mineral oil, 36 mg, 0.82 mmol) was added portionwise at RT to a solution of 3-methyl-4-(3-trifluoromethoxy-phenyl)-piperazin-2-one (150 mg, 0.55 mmol) in DMA (3 mL), then after 1 h a solution of 1-(3-chloropropyl)-piperidine in toluene [prepared from commercially available 1-(3-chloropropyl)-piperidine hydrochloride (542 mg, 2.74 mmol) by partitioning between toluene (4 ml) and 1 M aq. sodium hydroxide solution (4 ml) and drying of the organic layer with MgSO4] was added. The reaction mixture was heated at 75° C. for 1 h, then partitioned between sat. aq. NaHCO3 solution and CH2Cl2. The organic layer was dried (MgSO4), filtered, and evaporated. Chromatography (IST Isolute® Flash NH2; EtOAc) afforded the title compound (184 mg, 84%). Light yellow oil, MS: 400.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08138175B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-8d3832cdf33643f0b02bc38948c8353f |
|---|
| Source note | uspto-grants-2012_03 |
|---|