Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5521Generated: October 29, 2026

1-Methylpiperazine → HCID 178418611, compound

https://huagongshe.com/reaction/5521

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 numberUS05244890
Source datasetuspto-grants-1993_09
ORD IDord-267ddbce90734d2f82315bf163cec8db
Source noteuspto-grants-1993_09