HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245716Generated: October 26, 2026
Phosphorus oxychloride → 8-Chloro-3-(1-methylpiperidin-4-yl)imidazo[1,5-a]pyrazine
https://huagongshe.com/reaction/245716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-((3-chloropyrazin-2-yl)methyl)-1-methylpiperidine-4-carboxamide | HCID 86674656 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 8-Chloro-3-(1-methylpiperidin-4-yl)imidazo[1,5-a]pyrazine | HCID 86674657 | 91.9% |
Reaction Steps
To a solution of N-((3-chloropyrazin-2-yl)methyl)-1-methylpiperidine-4-carboxamide (6.51 mmol, 1.75 g) in acetonitrile (10 ml) was added phosphorus oxychloride (65.1 mmol, 6.36 ml) and this solution was heated at 80° C. for four hours. The reaction mixture was concentrated in vacuo and coevaporated with toluene. The residue was cooled in an ice bath and quenched with 7N ammonia in methanol (50 ml) and dichloromethane (50 ml). The solids were removed by filtration and the filtrate was concentrated. To the residue dichloromethane (50 ml) and of 7N ammonia in methanol (1 ml) was added. After 10 minutes at room temperature the solids were removed by filtration and the filtrate was concentrated. To the residue dichloromethane (50 ml) was added. After 10 minutes at room temperature the solids were removed by filtration and the filtrate was concentrated to give 8-chloro-3-(1-methylpiperidin-4-yl)imidazo[1,5-a]pyrazine (1.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08658794B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-db5e67fc968947a3ac4dec8674119d31 |
|---|
| Source note | uspto-grants-2014_02 |
|---|