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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701280Generated: October 30, 2026

1-Methylpiperazine → HCID 20347480, compound

https://huagongshe.com/reaction/1701280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
ReactantHCID 12595981HCID 12595981—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20347480HCID 20347480—

Reaction Steps

A mixture of 3.40 g. of carbonyl diimidazole and 25 ml. of tetrahydrofuran is cooled and 4.32 g. of 1-o-aminobenzyl-2-pyrrolecarboxylic acid is added. The mixture is allowed to stand at 25°-30° C. for 30 minutes and 2.6 ml. of N-methylpiperazine is added. The mixture is allowed to stand 48 hours, then concentrated to about 1/2 volume and treated with ether. The mixture is filtered. The filtrate is evaporated to remove the solvent. The residue is treated with water and methylene chloride. The methylene chloride layer is separated and concentrated and further purified by partition chromatography giving 1-[1-(o-aminobenzyl)-2-pyrrolecarbonyl]-4-methylpiperazine as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04192803
Source datasetuspto-grants-1980_03
ORD IDord-bcc774138bcd4c11bb3645e733ad8e47
Source noteuspto-grants-1980_03