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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040902Generated: October 29, 2026

4-Methyl-1-piperazinecarbonyl chloride → [7-[2-(3-Chlorophenyl)ethynyl]-9-oxa-3,8-diazaspiro[4.4]non-7-en-3-yl]-pyrrolidin-1-yl-methanone

https://huagongshe.com/reaction/2040902

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-1-piperazinecarbonyl chlorideHCID 3016935—
Reactant{3-[(3-Chlorophenyl)ethynyl]-1-oxa-2,7-diazaspiro[4.4]non-2-en-7-yl}(4-methyl piperazin-1-yl)methanoneHCID 56644861—
Product[7-[2-(3-Chlorophenyl)ethynyl]-9-oxa-3,8-diazaspiro[4.4]non-7-en-3-yl]-pyrrolidin-1-yl-methanoneHCID 5749378372.8%

Reaction Steps

The title compound was synthesized using the method described for the compound of Example 104, replacing 1-pyrrolidincarbonyl chloride for 4-methyl-1-piperazinecarbonyl chloride. After the usual work-up procedure, the crude was purified by means of automated flash chromatography (SP01®TM-Biotage; CHCl3-1.4N methanolic ammonia 100:0.5) to afford an ivory solid. Yield: 72.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580962B2
Source datasetuspto-grants-2013_11
ORD IDord-4e319a6d9090495681509550a98f0a33
Source noteuspto-grants-2013_11