Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734265Generated: October 31, 2026

1-Methylpiperazine → HCID 178418611, compound

https://huagongshe.com/reaction/1734265

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 numberUS05532354
Source datasetuspto-grants-1996_07
ORD IDord-48bcb46c084546c18ec1b1ea95f2d6b4
Source noteuspto-grants-1996_07