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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517558Generated: October 30, 2026

Piperazine → 1-(4-((tetrahydro-2H-pyran-2-yloxy)methyl)pyridin-2-yl)piperazine

https://huagongshe.com/reaction/517558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-chloro-4-((tetrahydro-2H-pyran-2-yloxy)methyl)pyridineHCID 86090104—
SolventWaterHCID 962—
SolventDiisopropylethylamineHCID 81531—
Product1-(4-((tetrahydro-2H-pyran-2-yloxy)methyl)pyridin-2-yl)piperazineHCID 8671149880.2%

Reaction Steps

A solution of 2-chloro-4-((tetrahydro-2H-pyran-2-yloxy)methyl)pyridine (8.7 g, 38.2 mmol) and piperazine (16.4 g, 191 mmol) in DIEA (30 mL) was heated at 150° C. for 48 h. The reaction mixture was diluted with H2O (1000 mL), and the solution was extracted with DCM/MeOH (10/1, 3×400 mL). The combined organic layers were washed with H2O (100 mL), and brine (100 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel column chromatography (DCM:MeOH=15:1) to afford 1-(4-((tetrahydro-2H-pyran-2-yloxy)methyl)pyridin-2-yl) piperazine as yellow oil (8.5 g, 80%). MS (ES+) C15H23N3O2 requires: 277, found: 278[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115120B2
Source datasetuspto-grants-2015_08
ORD IDord-37099c0602e54ed6b01bdb8b973bc3a2
Source noteuspto-grants-2015_08