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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609663Generated: October 30, 2026

1-Methylpiperazine → HCID 178418611, compound

https://huagongshe.com/reaction/1609663

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 178418684HCID 178418684—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 178418611HCID 17841861117.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of 2-methoxycarbonyl-4-hydroxy-5-benzyloxypyridine (18.15 g) in N-methylpiperazine (21.04 g) was heated to 100° C. for 3.5 hours. The resulting viscous solution was cooled to room temperature, diluted with a mixture of chloroform (270 ml) and methanol (30 ml) and subjected to column chromatography on silica gel (800 g) . The eluate was evaporated in vacuo and the residue was purified by column chromatography on silica gel (600 g) . The pure fractions were evaporated in vacuo and the residue was pulverized with diisopropyl ether to give 1-methyl-4-(4-hydroxy-5-benzyloxy-2-pyridylcarbonyl)piperazine (3.99 g) .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401734
Source datasetuspto-grants-1995_03
ORD IDord-872ed97cf6fd47ea80d744738a971beb
Source noteuspto-grants-1995_03