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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890812Generated: November 1, 2026

Ethylene Glycol → tert-butyl 4-(1-methyl-1H-pyrazol-4-yl)-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1890812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Methyl-4-iodo-1H-pyrazoleHCID 2734773—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
CatalystCopper iodideHCID 83717—
SolventIsopropanolHCID 3776—
Producttert-butyl 4-(1-methyl-1H-pyrazol-4-yl)-3-oxopiperazine-1-carboxylateHCID 67153719—

Reaction Steps

tert-Butyl 3-oxopiperazine-1-carboxylate (0.164 g, 0.819 mmol) was suspended in isopropanol (3 mL) under an atmosphere of nitrogen and treated with 1-methyl-4-iodo-1H-pyrazole (0.204 g, 0.983 mmol, 1.20 equiv), ethylene glycol (0.051 g, 0.82 mmol, 1.0 equiv), copper iodide (0.031 g, 0.16 mmol, 0.20 equiv), and potassium phosphate (0.695 g, 3.28 mmol, 4.00 equiv), and placed into a preheated oil bath at 100° C. for 8 hours. The mixture was cooled to ambient temperature, concentrated in vacuo and the residue was dissolved in dichloromethane, washed with water, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (100:0 to 0:100 hexanes:ethyl acetate), providing the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507494B2
Source datasetuspto-grants-2013_08
ORD IDord-fafb75c317704ee8b599046f05fc0984
Source noteuspto-grants-2013_08