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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-((3-chloropyrazin-2-yl)methyl)-1-methylpiperidine-4-carboxamideHCID 86674656—
SolventAcetonitrileHCID 6342—
Product8-Chloro-3-(1-methylpiperidin-4-yl)imidazo[1,5-a]pyrazineHCID 8667465791.9%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658794B2
Source datasetuspto-grants-2014_02
ORD IDord-db5e67fc968947a3ac4dec8674119d31
Source noteuspto-grants-2014_02