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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390324Generated: October 25, 2026

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

https://huagongshe.com/reaction/390324

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 Conditions

Temperature100 °C

Reaction Steps

To a solution of tert-butyl 3-oxopiperazine-1-carboxylate (0.164 g, 0.819 mmol) in 3 mL of isopropanol under an atmosphere of nitrogen was added 1-methyl-4-iodo-1H-pyrazole (0.204 g, 0.983 mmol), ethylene glycol (0.051 g, 0.82 mmol), copper iodide (0.031 g, 0.16 mmol), and potassium phosphate (0.695 g, 3.28 mmol). The reaction was heated to 100° C. for 8 h, cooled to rt, and concentrated in vacuo. The residue was dissolved in dichloromethane, washed with water, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified via silica gel chromatography, eluting with 10-100% ethyl acetate in hexanes to provide tert-butyl 4-(1-methyl-1H-pyrazol-4-yl)-3-oxopiperazine-1-carboxylate that gave a mass ion (ES+) of 281.1 for [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383638B2
Source datasetuspto-grants-2013_02
ORD IDord-27925b556c4a41b292e75d427d8d1302
Source noteuspto-grants-2013_02